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Barth syndrome.

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6 July 2020

Barth syndrome (English)

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23 February 2020

Ruth Newbury-Ecob

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Ruth Newbury-Ecob

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23 February 2020

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Ann Bowron

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Iris L Gonzalez

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Sarah J Groves

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Nicol Clayton

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Robin P Martin

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Beverly Tsai-Goodman

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Vanessa Garratt

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Michael Ashworth

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Valerie M Bowen

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Katherine R McCurdy

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Michaela K Damin

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Carolyn T Spencer

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Matthew J Toth

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Richard I Kelley

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publication date

12 February 2013

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23 February 2020

6 July 2020

Orphanet Journal of Rare Diseases

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23 February 2020

copyright license

Creative Commons Attribution 2.0 Generic

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copyright status

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on focus list of Wikimedia project

0 references

https://scigraph.springernature.com/pub.10.1186/1750-1172-8-23

0 references

Cardiac and skeletal muscle defects in a mouse model of human Barth syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

20 March 2017

Barth syndrome: an X-linked cause of fetal cardiomyopathy and stillbirth

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

20 March 2017

Cardiolipin and electron transport chain abnormalities in mouse brain tumor mitochondria: lipidomic evidence supporting the Warburg theory of cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

20 March 2017

Comparison of lymphoblast mitochondria from normal subjects and patients with Barth syndrome using electron microscopic tomography

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

20 March 2017

Monolysocardiolipin in cultured fibroblasts is a sensitive and specific marker for Barth Syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

20 March 2017

Mutation of DNAJC19, a human homologue of yeast inner mitochondrial membrane co-chaperones, causes DCMA syndrome, a novel autosomal recessive Barth syndrome-like condition

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

20 March 2017

Defective remodeling of cardiolipin and phosphatidylglycerol in Barth syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

20 March 2017

Barth syndrome may be due to an acyltransferase deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

20 March 2017

Clinical characterization of left ventricular noncompaction in children: a relatively common form of cardiomyopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

20 March 2017

Barth syndrome diagnosed in the subclinical stage of heart failure based on the presence of lipid storage myopathy and isolated noncompaction of the ventricular myocardium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

20 March 2017

Monolysocardiolipins accumulate in Barth syndrome but do not lead to enhanced apoptosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

20 March 2017

Barth syndrome: TAZ gene mutations, mRNAs, and evolution

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

20 March 2017

X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): an update

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

20 March 2017

A novel X-linked gene, G4.5. is responsible for Barth syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

20 March 2017

The biosynthesis and functional role of cardiolipin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

7 April 2017

Tafazzin knockdown in mice leads to a developmental cardiomyopathy with early diastolic dysfunction preceding myocardial noncompaction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

Seven functional classes of Barth syndrome mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

New mutation of mitochondrial DNAJC19 causing dilated and noncompaction cardiomyopathy, anemia, ataxia, and male genital anomalies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

Higher IL-6 and IL6:IGF Ratio in Patients with Barth Syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

Barth syndrome in a female patient

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

Cardiolipin affects the supramolecular organization of ATP synthase in mitochondria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

The 3-methylglutaconic acidurias: what's new?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

Fetal sex determination using circulating cell-free fetal DNA (ccffDNA) at 11 to 13 weeks of gestation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

Reduction in cholesterol synthesis in response to serum starvation in lymphoblasts of a patient with Barth syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

Mitochondrial cardiolipin involved in outer-membrane protein biogenesis: implications for Barth syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

Dysmorphology of Barth syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

Cardiolipin and mitochondrial carriers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

Distinct effects of tafazzin deletion in differentiated and undifferentiated mitochondria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

Mitochondrial defects lie at the basis of neutropenia in Barth syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

Use of modified cornstarch therapy to extend fasting in glycogen storage disease types Ia and Ib.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

Bloodspot assay using HPLC-tandem mass spectrometry for detection of Barth syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

Acute metabolic decompensation and sudden death in Barth syndrome: report of a family and a literature review.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

Successful cardiac transplantation in Barth syndrome--single-centre experience of four patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

Barth syndrome is associated with a cognitive phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

Cardiolipin: setting the beat of apoptosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

Cardiac features of a novel autosomal recessive dilated cardiomyopathic syndrome due to defective importation of mitochondrial protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

New insights into the regulation of cardiolipin biosynthesis in yeast: implications for Barth syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

A Drosophila model of Barth syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

Cardiac and clinical phenotype in Barth syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

Cardiolipin metabolism and Barth Syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

Ventricular arrhythmia in the X-linked cardiomyopathy Barth syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

Characterization of lymphoblast mitochondria from patients with Barth syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

Neutrophils in Barth syndrome (BTHS) avidly bind annexin-V in the absence of apoptosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

Phospholipid abnormalities in children with Barth syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

Deficiency of tetralinoleoyl-cardiolipin in Barth syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

Genetic analysis of the G4.5 gene in families with suspected Barth syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

X chromosome inactivation in carriers of Barth syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

Neonatal, lethal noncompaction of the left ventricular myocardium is allelic with Barth syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

Xq28-linked noncompaction of the left ventricular myocardium: prenatal diagnosis and pathologic analysis of affected individuals

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

Barth syndrome: clinical features and confirmation of gene localisation to distal Xq28.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

Dilated cardiomyopathy due to type II X-linked 3-methylglutaconic aciduria: successful treatment with pantothenic acid

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

Mapping of the locus for X-linked cardioskeletal myopathy with neutropenia and abnormal mitochondria (Barth syndrome) to Xq28

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

X-linked dilated cardiomyopathy with neutropenia, growth retardation, and 3-methylglutaconic aciduria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

Defects of the mitochondrial respiratory chain complexes in three pediatric cases with hypotonia and cardiac involvement

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

29 September 2017

Intrafamilial variability for novel TAZ gene mutation: Barth syndrome with dilated cardiomyopathy and heart failure in an infant and left ventricular noncompaction in his great-uncle

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

2 June 2018

Gonadal mosaicism of a TAZ (G4.5) mutation in a Japanese family with Barth syndrome and left ventricular noncompaction

1 reference

https://api.crossref.org/works/10.1186%2F1750-1172-8-23

21 January 2018

Cardiolipin and monolysocardiolipin analysis in fibroblasts, lymphocytes, and tissues using high-performance liquid chromatography-mass spectrometry as a diagnostic test for Barth syndrome.

1 reference

https://api.crossref.org/works/10.1186%2F1750-1172-8-23

21 January 2018

A zebrafish model of human Barth syndrome reveals the essential role of tafazzin in cardiac development and function

1 reference

https://api.crossref.org/works/10.1186%2F1750-1172-8-23

21 January 2018

The Epidemiology of Childhood Cardiomyopathy in Australia

1 reference

https://api.crossref.org/works/10.1186%2F1750-1172-8-23

21 January 2018

Barth syndrome: clinical observations and genetic linkage studies.

1 reference

https://api.crossref.org/works/10.1186%2F1750-1172-8-23

21 January 2018

Stroke associated with Barth syndrome.

1 reference

https://api.crossref.org/works/10.1186%2F1750-1172-8-23

21 January 2018

Barth syndrome associated with compound hemizygosity and heterozygosity of the TAZ and LDB3 genes.

1 reference

https://api.crossref.org/works/10.1186%2F1750-1172-8-23

21 January 2018

Long-term treatment of Barth syndrome with pantothenic acid: a retrospective study

1 reference

https://api.crossref.org/works/10.1186%2F1750-1172-8-23

21 January 2018

Earliest gestational age for fetal sexing in cell-free maternal plasma.

1 reference

https://api.crossref.org/works/10.1186%2F1750-1172-8-23

21 January 2018

Clinicopathologic conference: Barth Syndrome

1 reference

https://api.crossref.org/works/10.1186%2F1750-1172-8-23

21 January 2018

X-linked fetal cardiomyopathy caused by a novel mutation in the TAZ gene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

27 November 2018

Barth syndrome without 3-methylglutaconic aciduria.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

27 November 2018

Cardiolipin prevents rate-dependent uncoupling and provides osmotic stability in yeast mitochondria.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

27 November 2018

Non-Epstein-Barr virus-associated T-cell lymphoma following cardiac transplantation for Barth syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3583704

27 November 2018

The Barth Syndrome Registry: Distinguishing disease characteristics and growth data from a longitudinal study

1 reference

https://pubmed.ncbi.nlm.nih.gov/23398819

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Impaired cardiac reserve and severely diminished skeletal muscle O₂ utilization mediate exercise intolerance in Barth syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/23398819

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal clinical expression of 3-methylglutaconic aciduria: Barth syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/23398819

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked cardioskeletal myopathy and neutropenia (Barth syndrome)-MIM 302060

1 reference

https://pubmed.ncbi.nlm.nih.gov/23398819

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An X-linked recessive cardiomyopathy with abnormal mitochondria

1 reference

https://pubmed.ncbi.nlm.nih.gov/23398819

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Left ventricular noncompaction cardiomyopathy in Barth syndrome: an example of an undulating cardiac phenotype necessitating mechanical circulatory support as a bridge to transplantation

1 reference

https://pubmed.ncbi.nlm.nih.gov/23398819

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Barth syndrome presenting with acute metabolic decompensation in the neonatal period

1 reference

https://pubmed.ncbi.nlm.nih.gov/23398819

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dilated cardiomyopathy with neutropenia, short stature, and abnormal carnitine metabolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/23398819

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnosis of Barth syndrome using a novel LC-MS/MS method for leukocyte cardiolipin analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/23398819

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prolonged QT interval in hypertrophic and dilated cardiomyopathy in children

1 reference

https://pubmed.ncbi.nlm.nih.gov/23398819

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel Alu-mediated Xq28 microdeletion ablates TAZ and partially deletes DNL1L in a patient with Barth syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/23398819

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1750-1172-8-23

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23398819%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

Dimensions Publication ID

0 references

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23398819%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23398819%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

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