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Browsing by Author Eibel, Hermann

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Deficiency of caspase recruitment domain family, member 11 (CARD11), causes profound combined immunodeficiency in human subjects.

Author(s)Stepensky, Polina; Keller, Baerbel; Buchta, Mary, et al
TypeJournal article
Date PublishedFeb-2013
Date Created-

A multimorphic mutation in IRF4 causes human autosomal dominant combined immunodeficiency

Author(s)Fornes, Oriol; Jia, Alicia; Kuehn, Hye Sun, et al
TypeJournal article
Date Published20-Jan-2023
Date Created-
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