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The patients with CD3γ deficiency can present with different clinical findings despite having the same homozygous mutation. We report three new CD3gamma‐deficient siblings from a consanguineous family with a combined T−B+NK+ immunodeficiency and their variable clinical and cellular phenotypes despite the same homozygous mutation of the CD3G gene (c.80‐1G>C). We also re‐evaluate a previously reported...
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