Clinical, Immunological, and Genetic Findings in Iranian Patients with MHC-II Deficiency: Confirmation of c.162delG RFXANK Founder Mutation in the Iranian Population. - Mousavi Khorshidi, Mohadese Sadat; Seeleuthner, Yoann; Chavoshzadeh, Zahra; Behfar, Maryam; Hamidieh, Amir Ali; Alimadadi, Hosein; Sherkat, Roya; Momen, Tooba; Behniafard, Nasrin; Eskandarzadeh, Shabnam; Mansouri, Mahboubeh; Behnam, Mahdiyeh; et al. (Journal of Clinical Immunology, 2023)