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

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dc.contributor.authorNouioua, Sonia
dc.contributor.authorHamadouche, Tarik
dc.contributor.authorFunalot, Benoit
dc.contributor.authorBernard, Rafaëlle
dc.contributor.authorBellatache, Nora
dc.contributor.authorBouderba, Radia
dc.contributor.authorGrid, Djamel
dc.contributor.authorAssami, Salima
dc.contributor.authorBenhassine, Traki
dc.contributor.authorLevy, Nicolas
dc.contributor.authorVallat, Jean-Michel
dc.contributor.authorTazir, Meriem
dc.date.accessioned2015-06-15T12:33:18Z
dc.date.available2015-06-15T12:33:18Z
dc.date.issued2011
dc.identifier.issn09608966
dc.identifier.urihttps://dspace.univ-boumerdes.dz123456789/1853
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.relation.ispartofseriesNeuromuscular Disorders/ Vol.21,N°8 (2011);pp. 543-550
dc.subjectARCMTen_US
dc.subjectCMT4B1en_US
dc.subjectCMT4Fen_US
dc.subjectMTMR2 and PRX genesen_US
dc.subjectVocal cord palsyen_US
dc.subjectSkeletal deformitiesen_US
dc.titleNovel mutations in the PRX and the MTMR2 genes are responsible for unusual Charcot-Marie-Tooth disease phenotypesen_US
dc.typeArticleen_US

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