A molecular basis for familial hypertrophic cardiomyopathy: A β cardiac myosin heavy chain gene missense mutation-Reference-Cited by-同舟云学术

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A molecular basis for familial hypertrophic cardiomyopathy: A β cardiac myosin heavy chain gene missense mutation

Published:1990-09 Issue:5 Volume:62 Page:999-1006
ISSN:0092-8674
Container-title:Cell
language:en
Short-container-title:Cell

Author:

Geisterfer-Lowrance Anja A.T.,Kass Susan,Tanigawa Gary,Vosberg Hans-Peter,McKenna William,Seidman Christine E.,Seidman J.G.

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

Reference39 articles.

1. Current Protocols in Molecular Biology;Ausubel,1989

2. Type 1 fiber abnormalities in skeletal muscle of patients with hypertrophic and dilated cardiomyopathy: evidence of subclinical myogenic myopathy;Caforio;J. Am. Coll. Cardiol.,1989

3. Expression of recessive alleles by chromosomal mechanisms in retinoblastoma;Cavenee;Nature,1983

4. Familial prevalence and genetic transmission of idiopathic hypertrophic subaortic stenosis;Clark;N. Engl. J. Med.,1973

5. A reconstructive analysis of cell lineages;Darnell,1986

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