XIAP deficiency: a unique primary immunodeficiency best classified as X-linked familial hemophagocytic lymphohistiocytosis and not as X-linked lymphoproliferative disease
published in: Blood
date of publication: 2010-08-19
language: English
main subject: cell biology, familial hemophagocytic lymphohistiocytosis
Cites articles 26
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Article - wd:Q24610800