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Exome sequencing in multiplex autism families suggests a major role for heterozygous truncating mutations

dc.contributor.authorToma, Claudio
dc.contributor.authorTorrico, Bárbara
dc.contributor.authorHervas, Amaia
dc.contributor.authorValdés Mas, Rafael María 
dc.contributor.authorTristan-Noguero, A.
dc.contributor.authorPadillo, V.
dc.contributor.authorMaristany, M.
dc.contributor.authorSalgado, Marta
dc.contributor.authorArenas, C.
dc.contributor.authorSuárez Puente, Xosé Antón 
dc.contributor.authorBayés, Mónica
dc.contributor.authorCormand, B.
dc.date.accessioned2015-08-31T10:03:52Z
dc.date.available2015-08-31T10:03:52Z
dc.date.issued2014
dc.identifier.citationMolecular Psychiatry, 19(7), p. 784-790 (2014); doi:10.1038/mp.2013.106
dc.identifier.issn1359-4184
dc.identifier.issn1476-5578
dc.identifier.urihttp://hdl.handle.net/10651/32996
dc.description.sponsorshipEuropean Union [PIEF-GA-2009-254930]; AGAUR [2009SGR00971]; Fundacio La Marato de TV3 [092010]; Fundacion Alicia Koplowitz; Ministerio de Economia y Competitividad, Spain [SAF2012-33484, SAF2010-21165]
dc.format.extentp. 784-790
dc.language.isoeng
dc.relation.ispartofMolecular Psychiatry
dc.rights©,
dc.sourceWOS:000338185300007
dc.titleExome sequencing in multiplex autism families suggests a major role for heterozygous truncating mutations
dc.typeinfo:eu-repo/semantics/article
dc.identifier.local20142126
dc.identifier.doi10.1038/mp.2013.106
dc.type.dcmitext
dc.relation.publisherversionhttp://dx.doi.org/10.1038/mp.2013.106


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