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

dc.contributor.authorEstévez, A. R.
dc.contributor.authorPérez Nanclares, G.
dc.contributor.authorFernández Toral, Joaquín 
dc.contributor.authorRivas Crespo, Maximiliano Francisco 
dc.contributor.authorLópez Siguero, J. P.
dc.contributor.authorDíez, I.
dc.contributor.authorGrau, G.
dc.contributor.authorCastaño, Luis
dc.date.accessioned2015-12-21T10:39:57Z
dc.date.available2015-12-21T10:39:57Z
dc.date.issued2015
dc.identifier.citationJournal of Pediatric Endocrinology and Metabolism, 28(42286), p. 1129-1137 (2015); doi:10.1515/jpem-2014-0472
dc.identifier.issn0334-018X
dc.identifier.urihttp://hdl.handle.net/10651/34132
dc.format.extentp. 1129-1137
dc.language.isoeng
dc.relation.ispartofJournal of Pediatric Endocrinology and Metabolism
dc.rights©,
dc.sourceScopus
dc.source.urihttp://www.scopus.com/inward/record.url?eid=2-s2.0-84941113564&partnerID=40&md5=49f7fdaecb5e83831b8638368f14a04c
dc.titleClinical and molecular characterization of five Spanish kindreds with X-linked adrenal hypoplasia congenita: Atypical findings and a novel mutation in NR0B1
dc.typejournal article
dc.identifier.doi10.1515/jpem-2014-0472
dc.relation.publisherversionhttp://dx.doi.org/10.1515/jpem-2014-0472


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