ITK deficiency presenting as Autoimmune Lymphoproliferative Syndrome

A patient with a novel homozygous mutation in ITK presented with autoimmune lymphoproliferative syndrome, and had impaired TCR-driven Fas ligand upregulation, providing a mechanism for the T cell lymphoproliferation.

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:J Allergy Clin Immunol
Egile Nagusiak: Wallace, Jacqueline G, Alosaimi, Mohammed, Khayat, Claudia Djambas, Jaber, Faris, Almutairi, Abduarahman, Beaussant-Cohen, Sarah, Pinkus, Geraldine, Fleming, Mark, Mehawej, Cybel, Chou, Janet, Geha, Raif S
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2020
Gaiak:
Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC7779661/
https://ncbi.nlm.nih.gov/pubmed/32628964
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jaci.2020.06.019
Etiketak: Etiketa erantsi
Etiketarik gabe, Izan zaitez lehena erregistro honi etiketa jartzen!

Antzeko izenburuak