Clinical, Immunological, and Genetic Findings in Iranian Patients with MHC-II Deficiency: Confirmation of c.162delG RFXANK Founder Mutation in the Iranian Population.
Journal of clinical immunology | 2023-11-01 | PMID 37584719
Mousavi Khorshidi Mohadese Sadat, Seeleuthner Yoann, Chavoshzadeh Zahra and 21 more
