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

Karadima, G; Panas, M; Floroskufi, P; Kalfakis, N; Vassilopoulos, D

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	http://hdl.handle.net/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