(Q33873859)

29 July 2017

title

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

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ORCID Public Data File 2021

29 July 2017

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author name string

Cantlay AM

1

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29 July 2017

Shokrollahi K

2

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29 July 2017

Allen JT

3

1 reference

29 July 2017

Lunt PW

4

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29 July 2017

Newbury-Ecob RA

5

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29 July 2017

Steward CG

6

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29 July 2017

language of work or name

English

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publication date

1 September 1999

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The Journal of Pediatrics

29 July 2017

published in

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29 July 2017

volume

135

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29 July 2017

issue

3

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29 July 2017

page(s)

311-315

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

29 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2899%2970126-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2899%2970126-5

Barth syndrome: clinical observations and genetic linkage studies.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2899%2970126-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2899%2970126-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2899%2970126-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2899%2970126-5

Mutation characterization and genotype-phenotype correlation in Barth syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2899%2970126-5

Barth syndrome may be due to an acyltransferase deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2899%2970126-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2899%2970126-5

10.1016/S0022-3476(99)70126-5

7 January 2021

Identifiers

DOI

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29 July 2017

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