Clinical and molecular characterization of five Spanish kindreds with X-linked adrenal hypoplasia congenita: Atypical findings and a novel mutation in NR0B1

dc.contributor.author	Estévez, A. R.
dc.contributor.author	Pérez Nanclares, G.
dc.contributor.author	Fernández Toral, Joaquín
dc.contributor.author	Rivas Crespo, Maximiliano Francisco
dc.contributor.author	López Siguero, J. P.
dc.contributor.author	Díez, I.
dc.contributor.author	Grau, G.
dc.contributor.author	Castaño, Luis
dc.date.accessioned	2015-12-21T10:39:57Z
dc.date.available	2015-12-21T10:39:57Z
dc.date.issued	2015
dc.identifier.citation	Journal of Pediatric Endocrinology and Metabolism, 28(42286), p. 1129-1137 (2015); doi:10.1515/jpem-2014-0472
dc.identifier.issn	0334-018X
dc.identifier.uri	http://hdl.handle.net/10651/34132
dc.format.extent	p. 1129-1137
dc.language.iso	eng
dc.relation.ispartof	Journal of Pediatric Endocrinology and Metabolism
dc.rights	©,
dc.source	Scopus
dc.source.uri	http://www.scopus.com/inward/record.url?eid=2-s2.0-84941113564&partnerID=40&md5=49f7fdaecb5e83831b8638368f14a04c
dc.title	Clinical and molecular characterization of five Spanish kindreds with X-linked adrenal hypoplasia congenita: Atypical findings and a novel mutation in NR0B1
dc.type	journal article
dc.identifier.doi	10.1515/jpem-2014-0472
dc.relation.publisherversion	http://dx.doi.org/10.1515/jpem-2014-0472

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