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收藏Mutations in GDAP1 -: Autosomal recessive CMT with demyelination and axonopathy
Nelis, E; Erdem, S; Van den Bergh, PYK; Belpaire-Dethiou, MC; Ceuterick, C; Van Gerwen, V; Cuesta, A; Pedrola, L; Palau, F; Gabreëls-Festen, AAWM; Verellen, C; Tan, E; Demirci, M; Van Broeckhoven, C; De Jonghe, P; Topaloglu, H; Timmerman, V
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收藏The spectrum of mutations causing end-plate acetylcholinesterase deficiency
Ohno, K; Engel, AG; Brengman, JM; Shen, XM; Heidenreich, F; Vincent, A; Milone, M; Tan, E; Demirci, M; Walsh, P; Nakano, S; Akiguchi, I
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