Specific antibody deficiency and autoinflammatory disease extend the clinical and immunological spectrum of heterozygous NFKB1 loss-of-function mutations in humans.
نویسندگان
چکیده
Citation: Schipp C, Nabhani S, Bienemann K, Simanovsky N, Kfir-Erenfeld S, Assayag-Asherie N, Oommen PT, Revel-Vilk S, Hönscheid A, Gombert M, Ginzel S, Schäfer D, Laws H-J, Yefenof E, Fleckenstein B, Borkhardt A, Stepensky P, and Fischer U. Specific antibody deficiency and autoinflammatory disease extend the clinical and immunological spectrum of heterozygous NFKB1 loss-of-function mutations in humans. Haematologica. 2016; 101:xxx doi:10.3324/haematol.2016.145136
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عنوان ژورنال:
- Haematologica
دوره 101 10 شماره
صفحات -
تاریخ انتشار 2016