A new mutation of the lamin A/C gene leading to autosomal dominant axonal neuropathy, muscular dystrophy, cardiac disease, and leuconychia
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G. Másson | C. Goizet | X. Ferrer | P. Richard | G. Bonne | R. Yaou | E. Hermosilla | R. Ben Yaou | A. Lagueny | G. Le Masson | M. Rouanet | L. Demay | S. Bouillot