Segregation analysis in families with Charcot-Marie-Tooth disease allows reclassification of putative disease causing mutations

dc.contributor.author	Østern, Rune André Helland
dc.contributor.author	Fagerheim, Toril
dc.contributor.author	Hjellnes, Helene
dc.contributor.author	Nygård, Bjørn
dc.contributor.author	Mellgren, Svein Ivar
dc.contributor.author	Nilssen, Øivind
dc.date.accessioned	2015-03-13T11:26:19Z
dc.date.available	2015-03-13T11:26:19Z
dc.date.issued	2014
dc.identifier.citation	BMC Medical Genetics 2014, 15:12	en_US
dc.identifier.cristinID	FRIDAID 1128672
dc.identifier.doi	10.1186/1471-2350-15-12
dc.identifier.issn	1471-2350
dc.identifier.uri	https://hdl.handle.net/10037/7485
dc.identifier.urn	URN:NBN:no-uit_munin_7075
dc.language.iso	eng	en_US
dc.publisher	BioMed Central	en_US
dc.rights.accessRights	openAccess
dc.subject	VDP::714	en_US
dc.subject	VDP::752	en_US
dc.title	Segregation analysis in families with Charcot-Marie-Tooth disease allows reclassification of putative disease causing mutations	en_US
dc.type	Journal article	en_US
dc.type	Tidsskriftartikkel	en_US
dc.type	Peer reviewed	en_US