Dilated cardiomyopathy: a genetic approach (Q42390693)

29 October 2017

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Dilated cardiomyopathy: a genetic approach (English)

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29 October 2017

dilated cardiomyopathy

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L Mestroni

1

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language of work or name

English

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publication date

1 March 1997

1 reference

29 October 2017

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29 October 2017

77

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29 October 2017

3

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29 October 2017

185-188

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Dilated cardiomyopathy associated with deficiency of the cytoskeletal protein metavinculin

29 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=484677

Genetic factors in dilated cardiomyopathy.

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=484677

Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23.

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=484677

Mapping a cardiomyopathy locus to chromosome 3p22-p25.

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=484677

Familial dilated cardiomyopathy in the United Kingdom

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=484677

Linkage of familial dilated cardiomyopathy to chromosome 9. Heart Muscle Disease Study Group.

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=484677

The Frequency of Familial Dilated Cardiomyopathy in a Series of Patients with Idiopathic Dilated Cardiomyopathy

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=484677

Localization of a gene responsible for familial dilated cardiomyopathy to chromosome 1q32.

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=484677

Brief report: deletion of the dystrophin muscle-promoter region associated with X-linked dilated cardiomyopathy.

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=484677

A Point Mutation in the 5' Splice Site of the Dystrophin Gene First Intron Responsible for X-Linked Dilated Cardiomyopathy

16 August 2018

1 reference

12 December 2020

A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1

1 reference

12 December 2020

Epidemiology of idiopathic dilated and hypertrophic cardiomyopathy. A population-based study in Olmsted County, Minnesota, 1975-1984

1 reference

12 December 2020

Clinical and pathologic study of familial dilated cardiomyopathy

1 reference

12 December 2020

Inherited idiopathic dilated cardiomyopathy with multiple deletions of mitochondrial DNA

1 reference

12 December 2020

X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus

1 reference

12 December 2020

Cardiac involvement in Becker muscular dystrophy.

1 reference

12 December 2020

Brief report: deficiency of a dystrophin-associated glycoprotein (adhalin) in a patient with muscular dystrophy and cardiomyopathy

1 reference

12 December 2020

Identifiers

DOI

10.1136/HRT.77.3.185

1 reference

29 October 2017

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PMC publication ID

484677

29 October 2017

PubMed publication ID

9093029

1 reference

PMC publication ID

484677