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

dc.contributor.author	Toma, Claudio
dc.contributor.author	Torrico, Bárbara
dc.contributor.author	Hervas, Amaia
dc.contributor.author	Valdés Mas, Rafael María
dc.contributor.author	Tristan-Noguero, A.
dc.contributor.author	Padillo, V.
dc.contributor.author	Maristany, M.
dc.contributor.author	Salgado, Marta
dc.contributor.author	Arenas, C.
dc.contributor.author	Suárez Puente, Xosé Antón
dc.contributor.author	Bayés, Mónica
dc.contributor.author	Cormand, B.
dc.date.accessioned	2015-08-31T10:03:52Z
dc.date.available	2015-08-31T10:03:52Z
dc.date.issued	2014
dc.identifier.citation	Molecular Psychiatry, 19(7), p. 784-790 (2014); doi:10.1038/mp.2013.106
dc.identifier.issn	1359-4184
dc.identifier.issn	1476-5578
dc.identifier.uri	http://hdl.handle.net/10651/32996
dc.description.sponsorship	European 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.extent	p. 784-790
dc.language.iso	eng
dc.relation.ispartof	Molecular Psychiatry
dc.rights	©,
dc.source	WOS:000338185300007
dc.title	Exome sequencing in multiplex autism families suggests a major role for heterozygous truncating mutations
dc.type	journal article
dc.identifier.local	20142126
dc.identifier.doi	10.1038/mp.2013.106
dc.relation.publisherversion	http://dx.doi.org/10.1038/mp.2013.106

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