Clinical, genetic, and therapeutic diversity in 2 patients with severe mevalonate kinase deficiency

dc.contributor.author	Couce Pico, María Luz
dc.contributor.author	Baña Souto, Ana Maria
dc.date.accessioned	2017-06-07T07:17:21Z
dc.date.available	2017-06-07T07:17:21Z
dc.date.issued	2012
dc.identifier.issn	0031-4005
dc.identifier.uri	http://hdl.handle.net/20.500.11940/4743
dc.language.iso	eng
dc.title	Clinical, genetic, and therapeutic diversity in 2 patients with severe mevalonate kinase deficiency
dc.type	Artigo	es
dc.authorsophos	Gomez, A R
dc.authorsophos	Couce, M L
dc.authorsophos	Garcia-Villoria, J
dc.authorsophos	Torres, A
dc.authorsophos	Souto, A B
dc.authorsophos	Yague, J
dc.authorsophos	Vilaseca, M A
dc.authorsophos	Ribes, A
dc.authorsophos	Arostegui, J I
dc.identifier.doi	10.1542/peds.2010-2192
dc.identifier.isi	300395100037
dc.identifier.pmid	22271696
dc.identifier.sophos	7883
dc.issue.number	2
dc.journal.title	PEDIATRICS
dc.organization	Servizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago - Complexo Hospitalario Universitario de Santiago::Pediatría
dc.page.initial	e535
dc.page.final	E539
dc.rights.accessRights	openAccess
dc.typesophos	Artículo Original
dc.volume.number	129

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