(Q77768830)

English

Infantile dilated X-linked cardiomyopathy, G4.5 mutations, altered lipids, and ultrastructural malformations of mitochondria in heart, liver, and skeletal muscle

scientific article published on 01 March 2002

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11896212%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

Infantile dilated X-linked cardiomyopathy, G4.5 mutations, altered lipids, and ultrastructural malformations of mitochondria in heart, liver, and skeletal muscle (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11896212%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

1 reference

based on heuristic

inferred from title

1

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8 December 2019

Harald H. H. Göring

3

object named as

Harald H H Göring

1 reference

Europe PubMed Central

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8 December 2019

author name string

Monica Tsoras

2

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8 December 2019

Peter Hug

4

1 reference

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8 December 2019

Gail Chuck

5

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8 December 2019

Esther Tombragel

6

1 reference

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8 December 2019

Catherine McGraw

7

1 reference

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8 December 2019

James Schlotman

8

1 reference

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8 December 2019

Michael A Ralston

9

1 reference

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8 December 2019

George Hug

10

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8 December 2019

publication date

1 March 2002

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8 December 2019

Laboratory Investigation

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8 December 2019

82

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8 December 2019

3

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8 December 2019

335-344

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8 December 2019

https://scigraph.springernature.com/pub.10.1038/labinvest.3780427

0 references

Some monomethyl-branched fatty acids from ruminant fats: open-tubular GLC separations and indications of substitution on even-numbered carbon.

1 reference

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7 January 2021

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inferred from DOI database lookup

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

1 reference

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7 January 2021

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X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): respiratory-chain abnormalities in cultured fibroblasts

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.3780427

7 January 2021

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Hemodynamic and myocyte mitochondrial ultrastructural abnormalities in arrhythmogenic right ventricular dysplasia

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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Mismatch amplification mutation assay (MAMA): application to the c-H-ras gene

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.3780427

7 January 2021

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The rate of spontaneous mutation of a human gene

1 reference

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7 January 2021

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Novel gene mutations in patients with left ventricular noncompaction or Barth syndrome

1 reference

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7 January 2021

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Mutation characterization and genotype-phenotype correlation in Barth syndrome

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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inferred from DOI database lookup

Strategies for multilocus linkage analysis in humans

1 reference

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7 January 2021

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Barth syndrome may be due to an acyltransferase deficiency

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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Defective remodeling of cardiolipin and phosphatidylglycerol in Barth syndrome

1 reference

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7 January 2021

based on heuristic

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