A novel homozygous Y140X mutation of ISG15 causes diverse type I interferonopathies in sibling patients with cutaneous lesions or recurrent parenchymal pneumonia

A novel homozygous Y140X mutation of ISG15 causes diverse type I interferonopathies in sibling patients with cutaneous lesions or recurrent parenchymal pneumonia

Copyright © 2023. Published by Elsevier Inc.

Détails bibliographiques
Publié dans:Clinical immunology (Orlando, Fla.). - 1999. - 257(2023) vom: 15. Dez., Seite 109844
Auteur principal: Xu, Qiling (Auteur)
Autres auteurs: Li, Wenyan, Zhao, Qian, Zhao, Lu, Lv, Ge, Sun, Gan, Gao, Yelei, Ding, Yuan, Zhang, Zhiyong, Zhou, Lina, Chen, Yongwen, Tang, Xuemei, Zhu, Jin, Zhao, Xiaodong, An, Yunfei
Format: Article en ligne
Langue:English
Publié: 2023
Accès à la collection:Clinical immunology (Orlando, Fla.)
Sujets:Case Reports Journal Article IFN-I IFN-stimulated gene 15 (ISG15) JAK inhibitor Recurrent Pneumonia STAT baricitinib ISP4442I3Y Cytokines plus... Interferons 9008-11-1 ISG15 protein, human 60267-61-0 Ubiquitins
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