Severe XLP phenotype caused by a novel intronic mutation int he SH2D1A gene

dc.contributor.author	Tóth, Beáta
dc.contributor.author	Soltész B
dc.contributor.author	Gyimesi, Edit
dc.contributor.author	Csorba G
dc.contributor.author	Veres A
dc.contributor.author	Lányi, Árpád
dc.contributor.author	Kovács, Gábor
dc.contributor.author	Maródi, László
dc.contributor.author	Erdős, Melinda
dc.date.accessioned	2016-12-22T16:12:35Z
dc.date.available	2016-12-22T16:12:35Z
dc.date.issued	2015
dc.identifier	84925511241
dc.identifier.citation	pagination=26-31; journalIssueNumber=1; journalVolume=35; journalTitle=JOURNAL OF CLINICAL IMMUNOLOGY;
dc.identifier.uri	http://repo.lib.semmelweis.hu//handle/123456789/2862
dc.identifier.uri	doi:10.1007/s10875-014-0117-1
dc.relation.ispartof	urn:issn:0271-9142
dc.title	Severe XLP phenotype caused by a novel intronic mutation int he SH2D1A gene
dc.type	Journal Article
dc.date.updated	2015-11-27T13:59:24Z
dc.language.rfc3066	en
dc.identifier.mtmt	2819721
dc.identifier.wos	000348805600005
dc.identifier.pubmed	25491288
dc.contributor.department	SE/AOK/K/II. Sz. Gyermekgyógyászati Klinika
dc.contributor.institution	Semmelweis Egyetem