论文信息 - Mutations in GDAP1: Autosomal recessive CMT with demyelination and axonopathy - 字舞流文

Mutations in GDAP1: Autosomal recessive CMT with demyelination and axonopathy

C. van Broeckhoven | F. Palau | V. Timmerman | E. Nelis | H. Topaloglu | P. de Jonghe | L. Pedrola | E. Tan | M. Demirci | P. V. D. Van den Bergh | V. van Gerwen | C. Ceuterick | C. Verellen | A. Cuesta | S. Erdem | A. Gabreëls-Festen | M.-Cl Belpaire-Dethiou | H. Topaloğlu