(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 dilated cardiomyopathy

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Familial aggregation of idiopathic dilated cardiomyopathy

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Mildly dilated congestive cardiomyopathy

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Familial idiopathic dilated cardiomyopathy

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Frequency of familial nature of dilated cardiomyopathy and usefulness of cardiac transplantation in this subset

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Clinical and pathologic study of familial dilated cardiomyopathy

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Familial dilated 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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Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNALeu(UUR)

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

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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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Mapping a cardiomyopathy locus to chromosome 3p22-p25.

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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 hypertrophic cardiomyopathy: a genetic model of cardiac hypertrophy

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7 January 2021

X-linked dilated cardiomyopathy

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7 January 2021

Segmental wall motion abnormalities in dilated cardiomyopathy: a common finding and good prognostic sign

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7 January 2021

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Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death

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7 January 2021

Familial cardiomyopathy

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7 January 2021

Familial dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2897%2900434-8

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

1 reference

14 March 2018

1 reference

14 March 2018