Unreported Missense Mutation in the Dimerization Domain of ADA2 Leads to ADA2 Deficiency Associated with Severe Oral Ulcers and Neutropenia in a Female Somalian Patient—Addendum to the Genotype-Phenotype Puzzle
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DOI: 10.1007/s10875-019-00700-w
Abstract: To the Editor, ADA2 (previously known as CECR1, cat eye syndrome chromosome region, candidate 1) mutations encoding adenosine deaminase 2 (ADA2) were found to cause the first molecularly defined monogenic vasculitis syndrome [1, 2]. Initial… read more here.
Keywords: dimerization domain; domain ada2; unreported missense; missense mutation ... See more keywords