Molecular study of congenital erythrocytosis in 70 unrelated patients revealed a potential causal mutation in less than half of the cases (Where is/are the missing gene(s)?)

dc.contributor.author	Fernández Lago, Carlos
dc.date.accessioned	2017-06-07T06:56:41Z
dc.date.available	2017-06-07T06:56:41Z
dc.date.issued	2013
dc.identifier.issn	0902-4441
dc.identifier.uri	http://hdl.handle.net/20.500.11940/848
dc.language.iso	eng
dc.title	Molecular study of congenital erythrocytosis in 70 unrelated patients revealed a potential causal mutation in less than half of the cases (Where is/are the missing gene(s)?)
dc.type	Artigo	es
dc.authorsophos	Bento, C.
dc.authorsophos	Almeida, H.
dc.authorsophos	Maia, T. M.
dc.authorsophos	Relvas, L.
dc.authorsophos	Oliveira, A. C.
dc.authorsophos	Rossi, C.
dc.authorsophos	Girodon, F.
dc.authorsophos	Fernandez-Lago, C.
dc.authorsophos	Aguado-Diaz, A.
dc.authorsophos	Fraga, C.
dc.authorsophos	Costa, R. M.
dc.authorsophos	Araujo, A. L.
dc.authorsophos	Silva, J.
dc.authorsophos	Vitoria, H.
dc.authorsophos	Miguel, N.
dc.authorsophos	Silveira, M. P.
dc.authorsophos	Martin-Nunez, G.
dc.authorsophos	Ribeiro, M. L.
dc.identifier.doi	10.1111/ejh.12170
dc.identifier.isi	325035000010
dc.identifier.pmid	23859443
dc.identifier.sophos	11515
dc.issue.number	4
dc.journal.title	EUROPEAN JOURNAL OF HAEMATOLOGY
dc.organization	Servizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de A Coruña - Complexo Hospitalario Universitario A Coruña::Hematoloxía clínica
dc.page.initial	361
dc.page.final	368
dc.rights.accessRights	openAccess
dc.typesophos	Artículo Original
dc.volume.number	91

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