Narrowing the Genetic Causes of Language Dysfunction in the 1q21.1 Microduplication Syndrome

dc.contributor.author	Benítez Burraco, Antonio
dc.contributor.author	Barcos Martínez, Montserrat
dc.contributor.author	Espejo Portero, Isabel
dc.contributor.author	Fernández Urquiza, Maite
dc.contributor.author	Torres Ruíz, Raúl
dc.contributor.author	Rodríguez Perales, Sandra
dc.contributor.author	Jiménez Romero, María Salud
dc.date.accessioned	2018-10-08T10:23:00Z
dc.date.available	2018-10-08T10:23:00Z
dc.date.issued	2018
dc.identifier.citation	Frontiers In Pediatrics, 6, p. 163- (2018); doi:10.3389/fped.2018.00163
dc.identifier.issn	2296-2360
dc.identifier.uri	http://hdl.handle.net/10651/48690
dc.description.sponsorship	We would like to thank the proband and his family for their participation in this research. Preparation of this work was supported by funds from the Spanish Ministry of Economy and Competitiveness (grant number FFI2016-78034-C2-2-P [AEI/FEDER,UE] to AB-B, with MJ-R, MB-M, and IE-P as members of the project).
dc.format.extent	p. 163-
dc.language.iso	eng
dc.relation.ispartof	Frontiers In Pediatrics, 6
dc.rights	© 2018 Benítez-Burraco et al.
dc.rights	CC Reconocimiento 4.0 Internacional
dc.rights.uri	http://creativecommons.org/licenses/by/4.0/
dc.source	WOS:000434176800001
dc.title	Narrowing the Genetic Causes of Language Dysfunction in the 1q21.1 Microduplication Syndrome
dc.type	journal article
dc.identifier.doi	10.3389/fped.2018.00163
dc.relation.projectID	MINECO/FEDER/FFI2016-78034-C2-2-P
dc.relation.publisherversion	http://dx.doi.org/10.3389/fped.2018.00163
dc.rights.accessRights	open access

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