Exome sequencing reveals mutations in MFN2 and GDAP1 in severe Charcot–Marie–Tooth disease

Publisher： John Wiley & Sons Inc

E-ISSN： 1529-8027|19|3|242-245

ISSN： 1085-9489

Source： JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, Vol.19, Iss.3, 2014-09, pp. : 242-245

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