Items where Author is "Keramatipour, M."

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(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

(2019) Genetic mutations and immunological features of severe combined immunodeficiency patients in Iran. Immunology Letters. pp. 70-78. ISSN 0165-2478

This list was generated on Thu May 8 18:56:58 2025 +0330.