Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy-Reference-Cited by-同舟云学术

Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy

Published:1997-08 Issue:4 Volume:16 Page:379-382
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Kimura Akinori,Harada Haruhito,Park Jeong-Euy,Nishi Hirofumi,Satoh Manatsu,Takahashi Megumi,Hiroi Shitoshi,Sasaoka Taishi,Ohbuchi Nobuhisa,Nakamura Takeyuki,Koyanagi Takeshi,Hwang Tae-Hong,Choo Jin-A,Chung Kyu-Sung,Hasegawa Akira,Nagai Ryozo,Okazaki Osamu,Nakamura Hiroshi,Matsuzaki Masunori,Sakamoto Tsuguya,Toshima Hironori,Koga Yoshinori,Imaizumi Tsutomu,Sasazuki Takehiko

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0897-379.pdf

Reference29 articles.

1. Maron, B.J., Bonow, R.O., Cannon, R.O., Leon, M.B. & Epstein, S.E. Hypertrophic cardiomyopathy: interrelations of clinical manifestations, pathophysiology, and therapy. N. Engl. J. Med. 316, 780–789 (1987).

2. Jarcho, J.A. et al. Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1. N. Engl. J. Med. 321, 1372–1378 (1989).

3. Geisterfer-Lowrance, A.A.T. et al. A molecular basis for familial hypertrophic cardiomyopathy: a β cardiac myosin heavy chain gene missense mutation. Cell 62, 999–1006 (1990).

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

5. Thierfelder, L. et al. α-Tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere. Cell 77, 701–712 (1994).

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