Compound heterozygous TYK2 mutations underlie primary immunodeficiency with T-cell lymphopenia

Compound heterozygous TYK2 mutations underlie primary immunodeficiency with T-cell lymphopenia

Abstract Complete tyrosine kinase 2 (TYK2) deficiency has been previously described in patients with primary immunodeficiency diseases. The patients were infected with various pathogens, including mycobacteria and/or viruses, and one of the patients developed hyper-IgE syndrome. A detailed immunolog...

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Auteurs principaux: Michiko Nemoto, Hiroyoshi Hattori, Naoko Maeda, Nobuhiro Akita, Hideki Muramatsu, Suzuko Moritani, Tomonori Kawasaki, Masami Maejima, Hirotaka Ode, Atsuko Hachiya, Wataru Sugiura, Yoshiyuki Yokomaku, Keizo Horibe, Yasumasa Iwatani
Format: article
Langue:EN
Publié: Nature Portfolio 2018
Sujets:
Medicine
R
Science
Q
Accès en ligne:https://doaj.org/article/c8e265b15bc749268f942c3db043f96f
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https://doaj.org/article/c8e265b15bc749268f942c3db043f96f

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