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A V38A mutation in X-linked Charcot-Marie-Tooth neuropathy with unusual clinical features

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dc.contributor.author Karadima, G en
dc.contributor.author Panas, M en
dc.contributor.author Floroskufi, P en
dc.contributor.author Kalfakis, N en
dc.contributor.author Vassilopoulos, D en
dc.date.accessioned 2014-03-01T11:45:52Z
dc.date.available 2014-03-01T11:45:52Z
dc.date.issued 2004 en
dc.identifier.issn 0340-5354 en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/37664
dc.subject.classification Clinical Neurology en
dc.subject.other CONNEXIN 32 en
dc.subject.other DISEASE en
dc.subject.other GENE en
dc.subject.other PHENOTYPE en
dc.subject.other DEAFNESS en
dc.title A V38A mutation in X-linked Charcot-Marie-Tooth neuropathy with unusual clinical features en
heal.type other en
heal.language English en
heal.publicationDate 2004 en
heal.publisher DR DIETRICH STEINKOPFF VERLAG en
heal.journalName JOURNAL OF NEUROLOGY en
dc.identifier.isi ISI:000189177500015 en
dc.identifier.volume 251 en
dc.identifier.issue 2 en
dc.identifier.spage 222 en
dc.identifier.epage 223 en


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