Clinical characteristics of sudden death victims in heritable (chromosome 1p1-1q1) conduction and myocardial disease (Q77579194)

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6 December 2019

title

Clinical characteristics of sudden death victims in heritable (chromosome 1p1-1q1) conduction and myocardial disease (English)

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6 December 2019

author name string

S D Nelson

1

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6 December 2019

E A Sparks

2

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6 December 2019

H L Graber

3

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6 December 2019

H Boudoulas

4

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6 December 2019

A A Mehdirad

5

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P Baker

6

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C Wooley

7

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6 December 2019

language of work or name

English

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publication date

1 November 1998

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Journal of the American College of Cardiology

6 December 2019

published in

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6 December 2019

volume

32

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6 December 2019

page(s)

1717-1723

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6 December 2019

issue

6

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Inherited cardiomyopathies

6 December 2019

cites work

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7 January 2021

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

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Molecular basis of familial cardiomyopathies

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Genetic approaches to cardiovascular disease. Supravalvular aortic stenosis, Williams syndrome, and long-QT syndrome.

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7 January 2021

Sudden death in hypertrophic cardiomyopathy: a profile of 78 patients

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Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease

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Genotype-phenotype correlations in hypertrophic cardiomyopathy. Insights provided by comparisons of kindreds with distinct and identical beta-myosin heavy chain gene mutations

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7 January 2021

Preclinical diagnosis of familial hypertrophic cardiomyopathy by genetic analysis of blood lymphocytes

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7 January 2021

Genetics of the long QT syndrome

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The spectrum of symptoms and QT intervals in carriers of the gene for the long-QT syndrome

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Right ventricular cardiomyopathy and sudden death in young people

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Familial occurrence of right ventricular dysplasia: a study involving nine families

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7 January 2021

A new locus for arrhythmogenic right ventricular cardiomyopathy (ARVD2) maps to chromosome 1q42-q43

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7 January 2021

Gene for progressive familial heart block type I maps to chromosome 19q13.

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7 January 2021

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

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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

Classification of death in antiarrhythmia trials

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7 January 2021

10.1016/S0735-1097(98)00424-0

Identifiers

DOI

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6 December 2019

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