(Q35249677)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382096%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382096%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382096%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

Patrizia D'Adamo

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382096%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

Andrew Green

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382096%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

author name string

L Fassone

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382096%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

A Gedeon

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382096%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

E A Janssen

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382096%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

P A Bolhuis

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382096%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

P G Barth

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382096%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

M Wilson

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382096%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

E Haan

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382096%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

K H Orstavik

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382096%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

M A Patton

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382096%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

E Zammarchi

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382096%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

M A Donati

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382096%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

D Toniolo

15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382096%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

language of work or name

English

0 references

publication date

1 October 1997

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382096%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Human Genetics

7 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382096%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

volume

61

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382096%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

page(s)

862-867

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382096%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382096%20AND%20SRC:MED&resulttype=core&format=json

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

7 November 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715993

Molecular genetic insights into cardiovascular disease

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715993

Possible X linked congenital mitochondrial cardiomyopathy in three families

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715993

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715993

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715993

When cells stop making sense: effects of nonsense codons on RNA metabolism in vertebrate cells.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715993

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715993

Two cases of endocardial fibroelastosis--possible x-linked determination

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715993

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715993

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715993

Barth syndrome: clinical observations and genetic linkage studies.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715993

26 September 2018

Identifiers

DOI

10.1086/514886

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382096%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382096%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

1 reference