Novel mutations in the PRX and the MTMR2 genes are responsible for unusual Charcot-Marie-Tooth disease phenotypes

Nouioua, SoniaHamadouche, TarikFunalot, BenoitBernard, RafaëlleBellatache, NoraBouderba, RadiaGrid, DjamelAssami, SalimaBenhassine, TrakiLevy, NicolasVallat, Jean-MichelTazir, Meriem2015-06-152015-06-15201109608966https://dspace.univ-boumerdes.dz123456789/1853enARCMTCMT4B1CMT4FMTMR2 and PRX genesVocal cord palsySkeletal deformitiesNovel mutations in the PRX and the MTMR2 genes are responsible for unusual Charcot-Marie-Tooth disease phenotypesArticle