A novel NEMO/IKBKG mutation identified in a primary immunodeficiency disorder with recurrent atypical mycobacterial infections

oleh: Elysha Kolitz, BA, Bahir Chamseddin, MD, Rosemary Son, PA-C, Travis Vandergriff, MD, Amy P. Hsu, BA, Steven Holland, MD, Richard C. Wang, MD, PhD

Format: Article
Diterbitkan: Elsevier 2021-01-01

Deskripsi

Subjek

hypomorphic mutation; IKBKG; mycobacterial infection; NEMO; primary immunodeficiency; primary immunodeficiency without ectodermal dysplasia