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Novel SPG11 mutations in Asian kindreds and disruption of spatacsin function in the zebrafish

dc.contributor.authorSouthgate, Len_US
dc.contributor.authorDafou, Den_US
dc.contributor.authorHoyle, Jen_US
dc.contributor.authorLi, Nen_US
dc.contributor.authorKinning, Een_US
dc.contributor.authorCritchley, Pen_US
dc.contributor.authorNemeth, AHen_US
dc.contributor.authorTalbot, Ken_US
dc.contributor.authorBindu, PSen_US
dc.contributor.authorSinha, Sen_US
dc.contributor.authorTaly, ABen_US
dc.contributor.authorRaghavendra, Sen_US
dc.contributor.authorMuller, Fen_US
dc.contributor.authorMaher, ERen_US
dc.contributor.authorTrembath, RCen_US
dc.date.accessioned2015-05-27T12:16:25Z
dc.date.available2010-03-16en_US
dc.date.issued2010-10en_US
dc.identifier.issn1364-6745en_US
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/7519
dc.format.extent379 - 389en_US
dc.relation.ispartofNEUROGENETICSen_US
dc.rightsThis article is published with open access at Springerlink.com
dc.subjectHereditary spastic paraplegiaen_US
dc.subjectSPG11en_US
dc.subjectMolecular geneticsen_US
dc.subjectZebrafish studiesen_US
dc.subjectHEREDITARY SPASTIC PARAPLEGIAen_US
dc.subjectTHIN CORPUS-CALLOSUMen_US
dc.subjectMOTOR-NEURON DEGENERATIONen_US
dc.subjectGENETIC-HETEROGENEITYen_US
dc.subjectPROTEINen_US
dc.subjectLOCUSen_US
dc.subjectFREQUENTen_US
dc.subjectIDENTIFICATIONen_US
dc.subjectIMPAIRMENTen_US
dc.subjectNEUROPATHYen_US
dc.titleNovel SPG11 mutations in Asian kindreds and disruption of spatacsin function in the zebrafishen_US
dc.typeArticle
dc.rights.holder© The Author(s) 2010
dc.identifier.doi10.1007/s10048-010-0243-8en_US
pubs.issue4en_US
pubs.notesNot knownen_US
pubs.volume11en_US


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