Inherited Cardiomyopathies as a Troponin Disease
Author:
Affiliation:
1. Department of Clinical Pharmacology, Kyushu University Graduate School of Medicine
Publisher
Physiological Society of Japan
Subject
General Medicine,Physiology
Link
https://www.jstage.jst.go.jp/article/jjphysiol/54/4/54_4_307/_pdf
Reference106 articles.
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3. 3. Kushwaha SS, Fallon JT, and Fuster V: Restrictive cardiomyopathy. N Engl J Med 336: 267–276, 1997
4. 4. Thierfelder L, Watkins H, MacRae C, Lamas R, McKenna W, Vosberg HP, Seidman JG, and Seidman CE: Alpha- tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere. Cell 77: 701–712, 1994
5. 5. Kamisago M, Sharma SD, DePalma SR, Solomon S, Sharma P, McDonough B, Smoot L, Mullen MP, Woolf PK, Wigle ED, Seidman JG, and Seidman CE: Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy. [see comment]. N Engl J Med 343: 1688–1696, 2000
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