Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathy.

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Published in J Mol Med (Berl) on March 01, 1998

Authors

J Flavigny1, P Richard, R Isnard, L Carrier, P Charron, G Bonne, J F Forissier, M Desnos, O Dubourg, M Komajda, K Schwartz, B Hainque

Author Affiliations

1: Biochimie B, and IFR de Physiopathologie et de Génétique Cardiovasculaire, Hôpital Pitié-Salpêtrière, Paris, France.

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