论文信息 - Novel UBQLN2 mutations linked to amyotrophic lateral sclerosis and atypical hereditary spastic paraplegia phenotype through defective HSP70-mediated proteolysis - 字舞流文

Novel UBQLN2 mutations linked to amyotrophic lateral sclerosis and atypical hereditary spastic paraplegia phenotype through defective HSP70-mediated proteolysis

V. Meininger | F. Salachas | M. Amador | S. Forlani | G. Stevanin | D. Bohl | P. Couratier | B. Fontaine | D. Seilhean | S. Saker | G. Lautrette | M. Nicol | S. Millecamps | S. Boillée | E. Teyssou | L. Chartier | C. Dussert | Mathilde Mairey | Roselina Lam | Carine Moigneu | T. Larmonier | Selma Machat | Sandra Da Barroca