Clinical, Molecular, and Functional Characterization of CLCN1 Mutations in Three Families with Recessive Myotonia Congenita
暂无分享,去创建一个
S. Portaro | C. Rodolico | A. Toscano | D. Conte Camerino | J. Desaphy | C. Altamura | O. Musumeci | P. Imbrici | G. Camerino | N. Licata