Neonatal cardiomyopathy in mice homozygous for the Arg403Gln mutation in the α cardiac myosin heavy chain gene-Reference-Cited by-同舟云学术

Neonatal cardiomyopathy in mice homozygous for the Arg403Gln mutation in the α cardiac myosin heavy chain gene

Published:1999-01-01 Issue:1 Volume:103 Page:147-153
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Fatkin Diane,Christe Michael E.,Aristizabal Orlando,McConnell Bradley K.,Srinivasan Shardha,Schoen Frederick J.,Seidman Christine E.,Turnbull Daniel H.,Seidman J.G.

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference42 articles.

1. Familial hypertrophic cardiomyopathy: a genetic model of cardiac hypertrophy

2. A Mouse Model of Familial Hypertrophic Cardiomyopathy

3. Characteristics and Prognostic Implications of Myosin Missense Mutations in Familial Hypertrophic Cardiomyopathy

4. Noninvasive, In Utero Imaging of Mouse Embryonic Heart Development With 40-MHz Echocardiography

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