Mutations in UBQLN2 are rare in French amyotrophic lateral sclerosis
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V. Meininger | F. Salachas | A. Brice | C. Cazeneuve | P. Corcia | W. Camu | L. Lacomblez | D. Seilhean | P. Pradat | G. Bruneteau | V. Danel-Brunaud | S. Millecamps | S. Boillée | E. Leguern | N. Forestier | N. Vandenberghe