(Q28177723)

English

Mutational analysis of the beta- and delta-sarcoglycan genes in a large number of patients with familial and sporadic dilated cardiomyopathy

scientific article (publication date: July 2003)

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scholarly article

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Mutational analysis of the beta- and delta-sarcoglycan genes in a large number of patients with familial and sporadic dilated cardiomyopathy (English)

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mutational analysis

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based on heuristic

inferred from title

dilated cardiomyopathy

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based on heuristic

inferred from title

Christiane Bouchier

3

object named as

Christiane Bouchier

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object named as

Eric Villard

8

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Philippe Charron

object named as

Philippe Charron

4

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7

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Michel Komajda

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Nicolas Sylvius

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Nicolas Sylvius

1

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ORCID Public Data File 2021

Laetitia Duboscq-Bidot

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object named as

Laetitia Duboscq-Bidot

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Abdelaziz Benaiche

5

object named as

Abdelaziz Benaiche

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author name string

Pascale Sébillon

6

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language of work or name

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publication date

1 July 2003

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American Journal of Medical Genetics Part A

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120A

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1

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8-12

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Autosomal dominant dilated cardiomyopathy with atrioventricular block: a lamin A/C defect-related disease

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20003

21 January 2018

Disruption of heart sarcoglycan complex and severe cardiomyopathy caused by beta sarcoglycan mutations

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20003

21 January 2018

Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20003

21 January 2018

Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20003

21 January 2018

Frequency and phenotypes of familial dilated cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20003

21 January 2018

Titin mutations as the molecular basis for dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20003

21 January 2018

Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20003

21 January 2018

Familial dilated cardiomyopathy in the United Kingdom

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20003

21 January 2018

Desmin mutation responsible for idiopathic dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20003

21 January 2018

Familial dilated cardiomyopathy: clinical features in French families.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20003

21 January 2018

Cardiac and skeletal actin gene mutations are not a common cause of dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20003

21 January 2018

When the message goes awry: disease-producing mutations that influence mRNA content and performance.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20003

21 January 2018

Guidelines for the study of familial dilated cardiomyopathies. Collaborative Research Group of the European Human and Capital Mobility Project on Familial Dilated Cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20003

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20003

21 January 2018

A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20003

21 January 2018

Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20003

21 January 2018

Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20003

21 January 2018

Actin mutations in dilated cardiomyopathy, a heritable form of heart failure

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20003

21 January 2018

Mutations that alter the surface charge of alpha-tropomyosin are associated with dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20003

21 January 2018

Metavinculin mutations alter actin interaction in dilated cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20003

21 January 2018

A new locus for autosomal dominant dilated cardiomyopathy identified on chromosome 6q12-q16

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20003

21 January 2018

Epidemiology of desmin and cardiac actin gene mutations in a european population of dilated cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20003

21 January 2018

The role of cytoskeletal proteins in cardiomyopathies

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20003

21 January 2018

Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20003

21 January 2018

Familial aggregation of idiopathic dilated cardiomyopathy: clinical features and pedigree analysis in 14 families

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20003

21 January 2018

Idiopathic Dilated Cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20003

21 January 2018

Dystrophinopathy, the expanding phenotype. Dystrophin abnormalities in X-linked dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20003

21 January 2018

Lamin A/C Gene Mutation Associated With Dilated Cardiomyopathy With Variable Skeletal Muscle Involvement

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20003

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20003

21 January 2018

Familial dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20003

21 January 2018

Mutational analysis of the cardiac actin gene in familial and sporadic dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20003

21 January 2018

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10.1002/AJMG.A.20003

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