Exome sequencing is a useful diagnostic tool for complicated forms of hereditary spastic paraplegia

dc.contributor.author	Sobrido Gómez, María Jesús
dc.contributor.author	Quintans Castro, Beatriz
dc.date.accessioned	2017-06-07T07:30:02Z
dc.date.available	2017-06-07T07:30:02Z
dc.date.issued	2014
dc.identifier.issn	0009-9163
dc.identifier.uri	http://hdl.handle.net/20.500.11940/7246
dc.language.iso	eng
dc.title	Exome sequencing is a useful diagnostic tool for complicated forms of hereditary spastic paraplegia
dc.type	Artigo	es
dc.authorsophos	Bettencourt, C
dc.authorsophos	Lopez-Sendon, JL
dc.authorsophos	Garcia-Caldentey, J
dc.authorsophos	Rizzu, P
dc.authorsophos	Bakker, IMC
dc.authorsophos	Shomroni, O
dc.authorsophos	Quintans, B
dc.authorsophos	Davila, JR
dc.authorsophos	Bevova, MR
dc.authorsophos	Sobrido, MJ
dc.authorsophos	Heutink, P
dc.authorsophos	de Yebenes, JG
dc.identifier.doi	10.1111/cge.12133
dc.identifier.isi	329511700011
dc.identifier.pmid	23438842
dc.identifier.sophos	16214
dc.issue.number	2
dc.journal.title	CLINICAL GENETICS
dc.organization	Consellería de Sanidade::Fundación pública Galega de Medicina Xenómica
dc.organization	Servizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago::IDIS.- Instituto de investigaciones sanitarias de Santiago
dc.page.initial	154
dc.page.final	158
dc.rights.accessRights	openAccess
dc.typesophos	Artículo Original
dc.volume.number	85

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