Two novel missense mutations in FGD4/FRABIN cause Charcot-Marie-Tooth type 4H (CMT4H)

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dc.contributor.authorBaudot, Cécile
dc.contributor.authorEsteve, Clothilde
dc.contributor.authorCastro, Christel
dc.contributor.authorPoitelon, Yannick
dc.contributor.authorMas, Camille
dc.contributor.authorHamadouche, Tarik
dc.contributor.authorEl-Rajab, Maryam
dc.contributor.authorLévy, Nicolas
dc.contributor.authorMegarbané, André
dc.contributor.authorDelague, Valérie
dc.date.accessioned2015-06-11T15:37:45Z
dc.date.available2015-06-11T15:37:45Z
dc.date.issued2012
dc.identifier.issn10859489
dc.identifier.urihttps://dspace.univ-boumerdes.dz123456789/1718
dc.language.isoenen_US
dc.publisherPeripheral Nerve Societyen_US
dc.relation.ispartofseriesJournal of the Peripheral Nervous System/ Vol.17, N°2 (2012);pp. 141-146
dc.subjectCharcot-Marie-Tooth diseaseen_US
dc.subjectDisease geneen_US
dc.subjectFRABINen_US
dc.subjectHomozygous mutationen_US
dc.subjectMissenseen_US
dc.subjectPeripheral nerveen_US
dc.titleTwo novel missense mutations in FGD4/FRABIN cause Charcot-Marie-Tooth type 4H (CMT4H)en_US
dc.typeArticleen_US

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