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Mitochondrial DNA defects in cardiomyopathy
scientific article published on 01 July 1998
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
25851396
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25851396%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
title
Mitochondrial DNA defects in cardiomyopathy
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
25851396
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25851396%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
author name string
J Marin-Garcia
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
25851396
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25851396%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
M J Goldenthal
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
25851396
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25851396%20AND%20SRC:MED&resulttype=core&format=json
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4 March 2020
publication date
1 July 1998
1 reference
stated in
Europe PubMed Central
PubMed publication ID
25851396
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25851396%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
published in
Cardiovascular Pathology
1 reference
stated in
Europe PubMed Central
PubMed publication ID
25851396
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25851396%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
volume
7
1 reference
stated in
Europe PubMed Central
PubMed publication ID
25851396
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25851396%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
issue
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
25851396
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25851396%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
page(s)
205-213
1 reference
stated in
Europe PubMed Central
PubMed publication ID
25851396
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25851396%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
cites work
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Crossref
reference URL
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7 January 2021
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Molecular genetic aspects of cardiomyopathy
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
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7 January 2021
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Cardiomyopathy and abnormal mitochondrial function
1 reference
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Crossref
reference URL
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7 January 2021
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inferred from DOI database lookup
Genotype and phenotype of severe mitochondrial cardiomyopathy: a recipient of heart transplantation and the genetic control
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7 January 2021
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inferred from DOI database lookup
Alterations of the mitochondrial respiratory chain in human dilated cardiomyopathy
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7 January 2021
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Impaired mitochondrial function in idiopathic dilated cardiomyopathy: biochemical and molecular analysis
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Endomyocardial biopsies for early detection of mitochondrial disorders in hypertrophic cardiomyopathies
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7 January 2021
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OXPHOS defects and mitochondrial DNA mutations in cardiomyopathy
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Crossref
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7 January 2021
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A Novel mtDNA Point Mutation in Maternally Inherited Cardiomyopathy
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7 January 2021
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Mitochondrial mutation in fatal infantile cardiomyopathy
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7 January 2021
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Mitochondrial tRNA(Ile) mutation in fatal cardiomyopathy
1 reference
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Crossref
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7 January 2021
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inferred from DOI database lookup
A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with maternally inherited cardiomyopathy.
1 reference
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Crossref
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7 January 2021
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A novel mitochondrial DNA point mutation associated with mitochondrial encephalocardiomyopathy.
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7 January 2021
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Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNALeu(UUR)
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
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7 January 2021
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Point mutations in mitochondrial DNA in patients with hypertrophic cardiomyopathy
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Crossref
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7 January 2021
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Novel mutations in mitochondrial cytochrome b in fatal post partum cardiomyopathy
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7 January 2021
based on heuristic
inferred from DOI database lookup
Multiple mitochondrial DNA deletions exist in cardiomyocytes of patients with hypertrophic or dilated cardiomyopathy
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Whole mitochondrial genome amplification reveals basal level multiple deletions in mtDNA of patients with dilated cardiomyopathy
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Specific mitochondrial DNA deletions in idiopathic dilated cardiomyopathy
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
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7 January 2021
based on heuristic
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Inherited idiopathic dilated cardiomyopathy with multiple deletions of mitochondrial DNA
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Crossref
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https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
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7 January 2021
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inferred from DOI database lookup
Seminars in medicine of the Beth Israel Hospital, Boston. Mitochondrial DNA and disease
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7 January 2021
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inferred from DOI database lookup
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Crossref
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7 January 2021
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inferred from DOI database lookup
Mitochondrial encephalomyopathies: what next?
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Crossref
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7 January 2021
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inferred from DOI database lookup
Use of single strand conformation polymorphism analysis to detect point mutations in human mitochondrial DNA
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Crossref
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7 January 2021
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inferred from DOI database lookup
Mutations in mitochondrial tRNA genes: a frequent cause of neuromuscular diseases
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7 January 2021
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inferred from DOI database lookup
A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.
1 reference
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Crossref
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7 January 2021
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Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation
1 reference
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reference URL
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7 January 2021
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1 reference
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7 January 2021
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inferred from DOI database lookup
Identification of point mutations by mispairing PCR as exemplified in MERRF disease
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7 January 2021
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inferred from DOI database lookup
Prognostic implications of novel beta cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy
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X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus
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Mitochondrial function in children with idiopathic dilated cardiomyopathy.
1 reference
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inferred from DOI database lookup
Clinical presentation of mitochondrial disorders in childhood.
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Leigh syndrome and hypertrophic cardiomyopathy in an infant with a mitochondrial DNA point mutation (T8993G).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Cardiac mitochondrial dysfunction in Leigh syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Two novel pathogenic mitochondrial DNA mutations affecting organelle number and protein synthesis. Is the tRNA(Leu(UUR)) gene an etiologic hot spot?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytochrome c oxidase deficiency in Leigh syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Myopathy and fatal cardiopathy due to cytochrome c oxidase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial cardiomyopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA mutations in cardiomyopathy: Combination of replacements yielding cysteine residues and tRNA mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Multiple populations of deleted mitochondrial DNA detected by a novel gene amplification method
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Detection of a specific mitochondrial DNA deletion in tissues of older humans
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Age-dependent increase in deleted mitochondrial DNA in the human heart: possible contributory factor to presbycardia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Association of mitochondrial DNA damage with aging and coronary atherosclerotic heart disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA deletions in dilated cardiomyopathy: a clinical study employing endomyocardial sampling
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Accumulation of somatic nucleotide substitutions in mitochondrial DNA associated with the 3243 A-to-G tRNA(leu)(UUR) mutation in encephalomyopathy and cardiomyopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Multiple mitochondrial DNA deletions in an elderly human individual
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Accumulation of deletions in MtDNA during tissue aging: analysis by long PCR
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Detection and analysis of mitochondrial DNA deletions by whole genome PCR.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A direct repeat is a hotspot for large-scale deletion of human mitochondrial DNA.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Nucleus-driven mutations of human mitochondrial DNA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Multiple mitochondrial DNA deletions associated with autosomal recessive ophthalmoplegia and severe cardiomyopathy.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Variation in mitochondrial DNA levels in muscle from normal controls. Is depletion of mtDNA in patients with mitochondrial myopathy a distinct clinical syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial myopathy of childhood associated with depletion of mitochondrial DNA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial toxicity of antiviral drugs
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Depletion of muscle mitochondrial DNA in AIDS patients with zidovudine-induced myopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial myopathy caused by long-term zidovudine therapy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Partial cytochrome c oxidase deficiency and cytoplasmic bodies in patients with zidovudine myopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cardiomyopathy Associated with Antiretroviral Therapy in Patients with HIV Infection: A Report of Six Cases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sequence and organization of the human mitochondrial genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Normal variants of human mitochondrial DNA and translation products: the building of a reference data base
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA(Leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Oxidative phosphorylation diseases and mitochondrial DNA mutations: diagnosis and treatment
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Response of patients in classes III and IV of cardiomyopathy to therapy in a blind and crossover trial with coenzyme Q10.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1054-8807%2897%2900101-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S1054-8807(97)00101-4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
25851396
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25851396%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
PubMed publication ID
25851396
1 reference
stated in
Europe PubMed Central
PubMed publication ID
25851396
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25851396%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
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