Cardiac myosin binding protein–C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy-Reference-Cited by-同舟云学术

Cardiac myosin binding protein–C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy

Published:1995-12 Issue:4 Volume:11 Page:438-440
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Bonne Gisèle,Carrier Lucie,Bercovici Josiane,Cruaud Corinne,Richard Pascale,Hainque Bernard,Gautel Mathias,Labeit Siegfried,James Michael,Beckmann Jacques,Weissenbach Jean,Vosberg Hans-Peter,Fiszman Marc,Komajda Michel,Schwartz Ketty

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1295-438.pdf

Reference29 articles.

1. Maron, B.J. et al. Hypertrophic cardiomyopathy: interrelations of clinical manifestations, pathophysiology, and therapy (first of two parts). New Engl. J. Med. 316, 780–789 (1987).

2. Jarcho, J.A. et al. Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14ql. New Engl. J. Med. 321, 1372–1378 (1989).

3. Watkins, H. et al. A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3. Nature Genet. 3, 333–337 (1993).

4. Thierfelder, L. et al. A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2. Proc. natn. Acad. Sci. U.S.A. 90, 6270–6274 (1993).

5. Carrier, L. et al. Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11. Nature Genet. 4, 311–313 (1993).

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