A new mutation in PRKAG2 gene causing hypertrophic cardiomyopathy with conduction system disease and muscular glycogenosis
暂无分享,去创建一个
N. Romero | J. Hogrel | P. Laforêt | D. Duboc | B. Hainque | J. Leroy | E. Lacène | T. Lavergne | P. Richard | C. Baussan | K. Wahbi | M. A. Said