(Q34238646)

31 July 2017

1 reference

title

Cellular pathology and pathogenic aspects of neuronal ceroid lipofuscinoses (English)

1 reference

31 July 2017

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Kida E

1

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31 July 2017

Golabek AA

series ordinal

2

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31 July 2017

Wisniewski KE

series ordinal

3

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31 July 2017

publication date

1 January 2001

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31 July 2017

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31 July 2017

volume

45

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31 July 2017

page(s)

35-68

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Evidence for lipase abnormality: high levels of free and triacylglycerol forms of unsaturated fatty acids in neuronal ceroid-lipofuscinosis tissue.

31 July 2017

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7 January 2021

The mechanism and functional roles of protein palmitoylation in the nervous system

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7 January 2021

Pigmentoarchitectonic pathology of the isocortex in juvenile neuronal ceroid-lipofuscinosis: Axonal enlargements in layer IIIab and cell loss in layer V

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7 January 2021

Ovine neuronal ceroid lipofuscinosis: a large animal model syntenic with the human neuronal ceroid lipofuscinosis variant CLN6.

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7 January 2021

Use of electrospray ionization mass spectrometry and tandem mass spectrometry to study binding of F0 inhibitors to ceroid lipofuscinosis protein, a model system for subunit c of mitochondrial ATP synthase

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7 January 2021

Activator protein deficient Gaucher's disease. A second patient with the newly identified lipid storage disorder

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7 January 2021

The subcellular location of the yeast Saccharomyces cerevisiae homologue of the protein defective in the juvenile form of Batten disease

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7 January 2021

Molecular genetics of palmitoyl-protein thioesterase deficiency in the U.S.

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7 January 2021

Anomalies of mitochondrial ATP synthase regulation in four different types of neuronal ceroid lipofuscinosis

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7 January 2021

Low molecular weight storage material in infantile ceroid lipofuscinosis (CLN1).

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7 January 2021

Identification of a tripeptidyl aminopeptidase in the anterior pituitary gland: effect on the chemical and biological properties of rat and bovine growth hormones

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https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Signalling functions of protein palmitoylation

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7 January 2021

Sequences of members of the human gene family for the c subunit of mitochondrial ATP synthase

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Tissue culture loading test with storage granules from animal models of neuronal ceroid-lipofuscinosis (Batten disease): testing their lysosomal degradability by normal and Batten cells.

1 reference

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7 January 2021

Follow-up study of subunit c of mitochondrial ATP synthase (SCMAS) in Batten disease and in unrelated lysosomal disorders.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Specific delay of degradation of mitochondrial ATP synthase subunit c in late infantile neuronal ceroid lipofuscinosis (Batten disease)

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Specific delay in the degradation of mitochondrial ATP synthase subunit c in late infantile neuronal ceroid lipofuscinosis is derived from cellular proteolytic dysfunction rather than structural alteration of subunit c

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Decreased lysosomal subunit c-degrading activity in fibroblasts from patients with late infantile neuronal ceroid lipofuscinosis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

A lysosomal proteinase, the late infantile neuronal ceroid lipofuscinosis gene (CLN2) product, is essential for degradation of a hydrophobic protein, the subunit c of ATP synthase.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Characterization of endopeptidase activity of tripeptidyl peptidase-I/CLN2 protein which is deficient in classical late infantile neuronal ceroid lipofuscinosis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

The sequence of the major protein stored in ovine ceroid lipofuscinosis is identical with that of the dicyclohexylcarbodiimide-reactive proteolipid of mitochondrial ATP synthase

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Structure, function and regulation of the vacuolar (H+)-ATPases

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

On the ultrastructural diversity and essence of residual bodies in neuronal ceroid-lipofuscinosis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Expression studies of CLN3 protein (battenin) in fusion with the green fluorescent protein in mammalian cells in vitro

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

CLN3 protein regulates lysosomal pH and alters intracellular processing of Alzheimer's amyloid-beta protein precursor and cathepsin D in human cells

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Infantile type of so-called neuronal ceroid-lipofuscinosis. Histological and electron microscopic studies

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Lysosomal storage of subunit c of mitochondrial ATP synthase in Batten's disease (ceroid-lipofuscinosis)

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Recent Biochemical and Genetic Advances in Our Understanding of Batten's Disease (Ceroid-Lipofuscinosis)

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Human palmitoyl protein thioesterase: evidence for lysosomal targeting of the enzyme and disturbed cellular routing in infantile neuronal ceroid lipofuscinosis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Cellular uptake of saposin (SAP) precursor and lysosomal delivery by the low density lipoprotein receptor-related protein (LRP).

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Lysosomal proteolysis of prosaposin, the precursor of saposins (sphingolipid activator proteins): its mechanism and inhibition by ganglioside

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Palmitoyl-protein thioesterase and the molecular pathogenesis of infantile neuronal ceroid lipofuscinosis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Disease-specific pathology in neurons cultured from sheep affected with ceroid lipofuscinosis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Intracellular trafficking of lysosomal membrane proteins.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Concentrations of an activator protein for sphingolipid hydrolysis in liver and brain samples from patients with lysosomal storage diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

The gene coding for a sphingolipid activator protein, SAP-1, is on human chromosome 10

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Isolation of a novel gene underlying batten disease, CLN3

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Developmental expression of palmitoyl protein thioesterase in normal mice

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

A model for Batten disease protein CLN3: functional implications from homology and mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Biosynthesis and intracellular targeting of the CLN3 protein defective in Batten disease

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Defective intracellular transport of CLN3 is the molecular basis of Batten disease (JNCL)

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

A novel assay for lysosomal pepstatin-insensitive proteinase and its application for the diagnosis of late-infantile neuronal ceroid lipofuscinosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Purification and characterization of bovine brain lysosomal pepstatin-insensitive proteinase, the gene product deficient in the human late-infantile neuronal ceroid lipofuscinosis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Studies of membrane association of CLN3 protein

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

In vitro culture of neurons from sheep with Batten disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Increased expression of subunit c of mitochondrial ATP synthase in brain tissue from neuronal ceroid lipofuscinoses and mucopolysaccharidosis cases but not in long-term fibroblast cultures.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Topographic variabilities of immunoreactivity to subunit c of mitochondrial ATP synthase and lectin binding in late infantile neuronal ceroid-lipofuscinosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Analysis of intracellular distribution and trafficking of the CLN3 protein in fusion with the green fluorescent protein in vitro

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Leukocytes in neuronal ceroid-lipofuscinoses: function and apoptosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Beta-protein immunoreactivity in brains of patients with neuronal ceroid lipofuscinosis: ultrastructural and biochemical demonstration.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Protein degradation in the endoplasmic reticulum

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Specific storage of subunit c of mitochondrial ATP synthase in lysosomes of neuronal ceroid lipofuscinosis (Batten's disease)

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

The Batten disease gene product (CLN3p) is a Golgi integral membrane protein

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Light and electron microscopic studies on subunit c in cultured fibroblasts in late infantile and juvenile Batten disease

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Apoptosis as the mechanism of neurodegeneration in Batten's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Delayed classic and protracted phenotypes of compound heterozygous juvenile neuronal ceroid lipofuscinosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Proteolytic processing patterns of prosaposin in insect and mammalian cells

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Protein targeting by tyrosine- and di-leucine-based signals: evidence for distinct saturable components

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

A 0.1-700 Hz current through a voltage-clamped pore: candidate protein for initiator of neural oscillations.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Ion pores made of mitochondrial ATP synthase subunit c in the neuronal plasma membrane and Batten disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Evidence for phosphorylation of CLN3 protein associated with Batten disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Mutations in the palmitoyl-protein thioesterase gene (PPT; CLN1) causing juvenile neuronal ceroid lipofuscinosis with granular osmiophilic deposits [published erratum appears in Hum Mol Genet 1998 Apr;7(4):765]

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Targeted disruption of the Cln3 gene provides a mouse model for Batten disease. The Batten Mouse Model Consortium [corrected]

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Characterization of the expressed genes for subunit c of mitochondrial ATP synthase in sheep with ceroid lipofuscinosis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Molecular basis of the neuronal ceroid lipofuscinoses: Mutations inCLN1,CLN2,CLN3, andCLN5

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

High levels of brain dolichols in neuronal ceroid-lipofuscinosis and senescence

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

The expression of late infantile neuronal ceroid lipofuscinosis (CLN2) gene product in human brains.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Purification and characterization of a tripeptidyl peptidase I from human osteoclastomas: evidence for its role in bone resorption

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Mitochondrial ATP synthase subunit c storage in the ceroid-lipofuscinoses (Batten disease)

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Storage bodies in the ceroid-lipofuscinoses (Batten disease): low-molecular-weight components, unusual amino acids and reconstitution of fluorescent bodies from non-fluorescent components

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Different patterns of hydrophobic protein storage in different forms of neuronal ceroid lipofuscinosis (NCL, Batten disease)

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Accumulation of sphingolipid activator proteins (SAPs) A and D in granular osmiophilic deposits in miniature Schnauzer dogs with ceroid-lipofuscinosis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Action of BTN1, the yeast orthologue of the gene mutated in Batten disease

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

The frequency of lysosomal storage diseases in The Netherlands.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

CLN3 defines a novel antiapoptotic pathway operative in neurodegeneration and mediated by ceramide

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Conformational and amino acid residue requirements for the saposin C neuritogenic effect

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Tripeptidyl-peptidase I is apparently the CLN2 protein absent in classical late-infantile neuronal ceroid lipofuscinosis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

The targeting of Lamp1 to lysosomes is dependent on the spacing of its cytoplasmic tail tyrosine sorting motif relative to the membrane

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Sphingolipid metabolism. Sphingoid analogs, sphingolipid activator proteins, and the pathology of the cell.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

CLN5, a novel gene encoding a putative transmembrane protein mutated in Finnish variant late infantile neuronal ceroid lipofuscinosis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Genetic and physical mapping of the CLN6 gene on chromosome 15q21-23.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Rat brain contains high levels of mannose-6-phosphorylated glycoproteins including lysosomal enzymes and palmitoyl-protein thioesterase, an enzyme implicated in infantile neuronal lipofuscinosis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Association of mutations in a lysosomal protein with classical late-infantile neuronal ceroid lipofuscinosis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Specific alterations in levels of mannose 6-phosphorylated glycoproteins in different neuronal ceroid lipofuscinoses

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Mutational analysis of the defective protease in classic late-infantile neuronal ceroid lipofuscinosis, a neurodegenerative lysosomal storage disorder

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Biochemical characterization of a lysosomal protease deficient in classical late infantile neuronal ceroid lipofuscinosis (LINCL) and development of an enzyme-based assay for diagnosis and exclusion of LINCL in human specimens and animal models

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Palmitoyl-protein thioesterase, an enzyme implicated in neurodegeneration, is localized in neurons and is developmentally regulated in rat brain

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Batten disease fibroblasts in culture accumulate mitochondrial ATP synthase subunit 9

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Turnover of F1F0-ATP synthase subunit 9 and other proteolipids in normal and Batten disease fibroblasts

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Prosaposin prevents programmed cell death of rat cerebellar granule neurons in culture.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Storage of saposins A and D in infantile neuronal ceroid-lipofuscinosis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Sphingolipid activator proteins in the neuronal ceroid-lipofuscinoses: an immunological study

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Sphingolipid activator proteins (SAPs) in neuronal ceroid lipofuscinoses (NCL).

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Structural analysis of saposin C and B. Complete localization of disulfide bridges

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Saposins and their interaction with lipids

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

A new gene, encoding an anion transporter, is mutated in sialic acid storage diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Lysosomal targeting of palmitoyl-protein thioesterase

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Purification and characterisation of a tripeptidyl aminopeptidase I from rat spleen

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Classical late infantile neuronal ceroid lipofuscinosis fibroblasts are deficient in lysosomal tripeptidyl peptidase I

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Topogenic signals in integral membrane proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Identification of three novel mutations of the palmitoyl-protein thioesterase-1 (PPT1) gene in children with neuronal ceroid-lipofuscinosis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Transmembrane domain mutations influence the cellular distribution of lysosomal membrane glycoprotein A

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Topographic heterogeneity of amyloid B-protein epitopes in brains with various forms of neuronal ceroid lipofuscinoses suggesting defective processing of amyloid precursor protein

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Altered amyloid beta-protein precursor processing in brains of patients with neuronal ceroid lipofuscinosis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Variability in the clinical and pathological findings in the neuronal ceroid lipofuscinoses: Review of data and observations

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

New subform of the late infantile form of neuronal ceroid lipofuscinosis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Increased urine concentration of subunit c of mitochondrial ATP synthase in neuronal ceroid lipofuscinoses patients.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Rapid detection of subunit c of mitochondrial ATP synthase in urine as a diagnostic screening method for neuronal ceroid-lipofuscinoses.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Studies of atypical JNCL suggest overlapping with other NCL forms.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Compound heterozygous genotype is associated with protracted juvenile neuronal ceroid lipofuscinosis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Identification of retinoyl complexes as the autofluorescent component of the neuronal storage material in Batten disease

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Sequence analysis and mapping of a novel human mitochondrial ATP synthase subunit 9 cDNA (ATP5G3)

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

Molecular screening of Batten disease: identification of a missense mutation (E295K) in the CLN3 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2801%2945003-6

7 January 2021

10.1016/S0065-2660(01)45003-6

Identifiers

DOI

1 reference

31 July 2017

1 reference