G.P.1 07 AMP-activated protein kinase gene mutation: a new cause of muscular glycogenosis associated with hypertrophic cardiomyopathy and conduction defect

✍ Scribed by P. Laforêt; P. Richard; M. Aït Saïd; N.B. Romero; E. Lacène; J.-P. Leroy; C. Baussan; J.-Y. Hogrel; T. Lavergne; K. Wahbi; B. Hainque; D. Duboc

• Book ID: 116792510
• Publisher: Elsevier Science
• Year: 2006
• Tongue: English
• Weight: 44 KB
• Volume: 16
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/j.nmd.2006.05.053