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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| Description | scientific article |
| Author/s |
author: Michel Komajda Philippe Charron Richard Isnard Gisèle Bonne |
| Publication date | March 1998 |
| Language | English |
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