Novel mutations of TYK2 leading to divergent clinical phenotypes

Lv, G; Sun, G; Wu, PL; Du, X; Zeng, T; Wen, W; Zhou, LN; An, YF; Tang, XM; He, TY; Zhao, XD; Du, HQ

Zhao, XD; Du, HQ (通讯作者),Chongqing Med Univ, Natl Clin Res Ctr Child Hlth & Disorders, Childrens Hosp, Chongqing 400000, Peoples R China.

PEDIATRIC ALLERGY AND IMMUNOLOGY, 2022; 33 (1):

Abstract

Background TYK2 deficiency is a rare primary immunodeficiency disease caused by loss-of-function mutations of TYK2 gene, which is initially proposed a......

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