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

Tóth, Beáta; Soltész B; Gyimesi, Edit; Csorba G; Veres A; Lányi, Árpád; Kovács, Gábor; Maródi, László; Erdős, Melinda
Journal article
JOURNAL OF CLINICAL IMMUNOLOGY vol.:35, issue.:1, p.:26-31.
ISSN: 0271-9142
URI: http://repo.lib.semmelweis.hu//handle/123456789/2862
10.1007/s10875-014-0117-1
xmlui.dri2xhtml.METS-1.0.item-mtmtid: 2819721
WoS ID: 000348805600005
PubMed ID: 25491288
Date: 2015

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