Frequency and phenotypes of familial dilated cardiomyopathy (Q50507089)

14 March 2018

title

Frequency and phenotypes of familial dilated cardiomyopathy (English)

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14 March 2018

6

Katus HA

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14 March 2018

author name string

Grünig E

1

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14 March 2018

Tasman JA

2

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14 March 2018

Kücherer H

3

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14 March 2018

Franz W

4

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14 March 2018

Kübler W

5

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14 March 2018

language of work or name

English

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publication date

1 January 1998

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14 March 2018

Journal of the American College of Cardiology

published in

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14 March 2018

volume

31

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14 March 2018

issue

1

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14 March 2018

page(s)

186-194

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14 March 2018

Dominant and recessive modes of inheritance in idiopathic cardiomyopathy

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

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

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

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

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

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Differences in clinical expression of hypertrophic cardiomyopathy associated with two distinct mutations in the beta-myosin heavy chain gene. A 908Leu----Val mutation and a 403Arg----Gln mutation

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7 January 2021

Familial dilated cardiomyopathy

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7 January 2021

Evolution of a hereditary cardiac conduction and muscle disorder: a study involving a family with six generations affected

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7 January 2021

10.1016/S0735-1097(97)00434-8

Identifiers

DOI

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14 March 2018

1 reference

14 March 2018