Browsing by Author Eibel, Hermann
Showing results 1 to 2 of 2
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 |
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Type | Journal article |
Date Published | Feb-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 |
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Type | Journal article |
Date Published | 20-Jan-2023 |
Date Created | - |
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