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

✍ Scribed by Jeanne Flavigny; Pascale Richard; Richard Isnard; Lucie Carrier; Philippe Charron; Gisèle Bonne; Jean-François Forissier; Michel Desnos; Olivier Dubourg; Michel Komajda; Ketty Schwartz; B. Hainque

• Publisher: Springer
• Year: 1998
• Tongue: English
• Weight: 434 KB
• Volume: 76
• Category: Article
• ISSN: 0946-2716
• DOI: 10.1007/s001090050210