(Q57907320)

Philippe Charron

3

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Viviane M. Conraads

Viviane Conraads

5

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Michel Komajda

7

Michel Komajda

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Laetitia Duboscq-Bidot

2

Laetitia Duboscq-Bidot

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Abdelaziz Benaiche

4

Abdelaziz Benaiche

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author name string

Nicolas Sylvius

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

6

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publication date

15 March 2005

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published in

European Heart Journal

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volume

26

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issue

8

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page(s)

794-803

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cites work

1 reference

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Familial dilated cardiomyopathy in the United Kingdom

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1 reference

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Frequency and phenotypes of familial dilated cardiomyopathy.

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Many roads lead to a broken heart: the genetics of dilated cardiomyopathy

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1 reference

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

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Metavinculin mutations alter actin interaction in dilated cardiomyopathy.

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The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathy

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1 reference

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Dilated cardiomyopathy and heart failure caused by a mutation in phospholamban

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A Cypher/ZASP mutation associated with dilated cardiomyopathy alters the binding affinity to protein kinase C.

21 January 2018

1 reference

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Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy

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Novel mutations in sarcomeric protein genes in dilated cardiomyopathy.

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Familial dilated cardiomyopathy: from clinical presentation to molecular genetics.

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1 reference

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

21 January 2018

1 reference

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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

21 January 2018

1 reference

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Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutations.

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1 reference

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

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Mutations of the light meromyosin domain of the beta-myosin heavy chain rod in hypertrophic cardiomyopathy

21 January 2018

1 reference

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Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy

21 January 2018

1 reference

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Cardiac troponin T lysine 210 deletion in a family with dilated cardiomyopathy

21 January 2018

1 reference

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Low sequence variation in the gene encoding the human beta-myosin heavy chain.

21 January 2018

1 reference

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

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1 reference

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Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy

21 January 2018

1 reference

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