Items where Author is "Cobat, A."

Article

(2023) Clinical, Immunological, and Genetic Findings in Iranian Patients with MHC-II Deficiency: Confirmation of c.162delG <i>RFXANK</i> Founder Mutation in the Iranian Population. Journal of Clinical Immunology. pp. 1941-1952. ISSN 0271-9142

(2023) Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency. The Journal of experimental medicine. ISSN 1540-9538 (Electronic) 0022-1007 (Print) 0022-1007 (Linking)

(2022) Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency. Journal of Experimental Medicine. p. 31. ISSN 0022-1007