Specific antibody deficiency and autoinflammatory disease extend the clinical and immunological spectrum of heterozygous NFKB1 loss-of-function mutations in humans

Schipp C, Nabhani S, Bienemann K, Simanovsky N, Kfir-Erenfeld S, Assayag-Asherie N, Oommen PT, Revel-Vilk S, Hoenscheid A, Gombert M, Ginzel S, Schaefer D, Laws HJ, Yefenof E, Fleckenstein B, Borkhardt A, Stepensky P, Fischer U (2016)

Publication Type: Journal article

Publication year: 2016

Journal

Haematologica Ferrata Storti Foundation

Book Volume: 101

Pages Range: e392-e396

Journal Issue: 10

DOI: 10.3324/haematol.2016.145136

Authors with CRIS profile

Bernhard Fleckenstein Lehrstuhl für Klinische und Molekulare Virologie

Involved external institutions

Hebrew University of Jerusalem IL Israel (IL) Heinrich-Heine-Universität Düsseldorf DE Germany (DE) Hadassah Medical Center / מרכז רפואי הדסה‎‎ IL Israel (IL)

How to cite

APA:

Schipp, C., Nabhani, S., Bienemann, K., Simanovsky, N., Kfir-Erenfeld, S., Assayag-Asherie, N.,... Fischer, U. (2016). Specific antibody deficiency and autoinflammatory disease extend the clinical and immunological spectrum of heterozygous NFKB1 loss-of-function mutations in humans. Haematologica, 101(10), e392-e396. https://doi.org/10.3324/haematol.2016.145136

MLA:

Schipp, Cyrill, et al. "Specific antibody deficiency and autoinflammatory disease extend the clinical and immunological spectrum of heterozygous NFKB1 loss-of-function mutations in humans." Haematologica 101.10 (2016): e392-e396.

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