Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1.
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F. Muntoni | K. Flanigan | S. Chin | H. Goebel | C. Bönnemann | M. Scavina | L. Bridges | K. Swoboda | R. Battini | C. Mitchell | J. Schessl | B. Maiti | C. Sewry | A. Taratuto | Ying Hu | Y. Zou | P. Standring | G. Espada | M. Saccoliti | A. Dubrovsky | M. Erro | Monica Robertella | P. Olmos