MYH9 disease: Identification of two mutations associated with uncommon clinical phenotype.

dc.date.accessioned	2017-06-07T07:24:29Z
dc.date.available	2017-06-07T07:24:29Z
dc.date.issued	2015
dc.identifier.issn	1538-7933
dc.identifier.uri	http://hdl.handle.net/20.500.11940/6061
dc.language.iso	eng
dc.title	MYH9 disease: Identification of two mutations associated with uncommon clinical phenotype.
dc.type	Publicación de congreso
dc.authorsophos	Guiu M.I.S.
dc.authorsophos	Muina B.
dc.authorsophos	Periago A.
dc.authorsophos	Albornoz D.J.
dc.authorsophos	Soler M.
dc.authorsophos	Vicente V.
dc.authorsophos	Lozano M.L.
dc.authorsophos	Rivera J.
dc.identifier.isi	356426903051
dc.identifier.sophos	19821
dc.journal.title	JOURNAL OF THROMBOSIS AND HAEMOSTASIS
dc.organization	Servizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Ourense - Complexo Hospitalario Universitario de Ourense
dc.rights.accessRights	openAccess
dc.typesophos	Comunicaciones a congresos
dc.volume.number	13

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