Clinical features of hypertrophic cardiomyopathy caused by a Lys183 deletion mutation in the cardiac troponin I gene.

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Published in Circulation on August 08, 2000

Authors

H Kokado1, M Shimizu, H Yoshio, H Ino, K Okeie, Y Emoto, T Matsuyama, M Yamaguchi, T Yasuda, N Fujino, H Ito, H Mabuchi

Author Affiliations

1: Second Department of Internal Medicine, School of Medicine, Kanazawa University, Kanazawa, Japan. fcc13@lilac.ocn.ne.jp

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