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Autosomal-dominant B-cell deficiency with alopecia due to a mutation in NFKB2 that results in nonprocessable p100

Lee, Cindy; Fulcher, David; Whittle, Belinda; Chand, Rochna; Fewings, Nicole; Field, Matthew; Andrews, Dan; Goodnow, Christopher; Cook, Matthew


Most genetic defects that arrest B-cell development in the bone marrow present early in life with agammaglobulinemia, whereas incomplete antibody deficiency is usually associated with circulating B cells. We report 3 related individuals with a novel form

CollectionsANU Research Publications
Date published: 2014
Type: Journal article
Source: Blood
DOI: 10.1182/blood-2014-06-578542


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