Genotypic and phenotypic spectrum of the most common causative genes of Charcot-Marie-Tooth disease in Hungarian patients

dc.contributor.author	György, Máté Milley
dc.contributor.author	Edina, Timea Varga
dc.contributor.author	Zoltán, Grosz
dc.contributor.author	Csilla, Nemes
dc.contributor.author	Zsuzsanna, Arányi
dc.contributor.author	Judit, Boczán
dc.contributor.author	Péter, Diószeghy
dc.contributor.author	Mária, Judit Molnár
dc.contributor.author	Anikó, Gál
dc.date.accessioned	2019-11-21T12:26:07Z
dc.date.available	2019-11-21T12:26:07Z
dc.date.issued	2018
dc.identifier	85034859869
dc.identifier.citation	journalVolume=28;journalIssueNumber=1;journalTitle=NEUROMUSCULAR DISORDERS;pagerange=38-38;journalAbbreviatedTitle=NEUROMUSCULAR DISORD;
dc.identifier.uri	http://repo.lib.semmelweis.hu//handle/123456789/7316
dc.identifier.uri	doi:10.1016/j.nmd.2017.08.007
dc.format.extent	38-43
dc.title	Genotypic and phenotypic spectrum of the most common causative genes of Charcot-Marie-Tooth disease in Hungarian patients
dc.type	Journal Article
dc.date.updated	2019-07-30T06:53:41Z
dc.language.rfc3066	en
dc.rights.holder	NULL
dc.identifier.mtmt	3302070
dc.identifier.wos	000427210600006
dc.identifier.pubmed	29174527
dc.contributor.institution	MTA-DE Sejtélettani Kutatócsoport (2006 végéig működött)
dc.contributor.institution	Neurológiai Klinika
dc.contributor.institution	Neurológiai Tanszék
dc.contributor.institution	Neurológiai Klinika
dc.contributor.institution	Genomikai Medicina és Ritka Betegségek Intézete
dc.contributor.institution	MTA-SE-NAP B Peripheriás idegrendszeri kutatócsoport