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Clinical, Immunological, and Genetic Findings in Iranian Patients with MHC-II Deficiency: Confirmation of c.162delG RFXANK Founder Mutation in the Iranian Population.

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Title: Clinical, Immunological, and Genetic Findings in Iranian Patients with MHC-II Deficiency: Confirmation of c.162delG RFXANK Founder Mutation in the Iranian Population.
Authors: Mousavi Khorshidi, Mohadese Sadat1 (AUTHOR), Seeleuthner, Yoann2,3 (AUTHOR), Chavoshzadeh, Zahra4 (AUTHOR), Behfar, Maryam5,6 (AUTHOR), Hamidieh, Amir Ali5,6 (AUTHOR), Alimadadi, Hosein7 (AUTHOR), Sherkat, Roya8 (AUTHOR), Momen, Tooba9 (AUTHOR), Behniafard, Nasrin10,11 (AUTHOR), Eskandarzadeh, Shabnam12 (AUTHOR), Mansouri, Mahboubeh4 (AUTHOR), Behnam, Mahdiyeh13,14 (AUTHOR), Mahdavi, Mohadese1 (AUTHOR), Heydarazad Zadeh, Maryam4 (AUTHOR), Shokri, Mehdi15 (AUTHOR), Alizadeh, Fatemeh1 (AUTHOR), Movahedi, Mahshid1 (AUTHOR), Momenilandi, Mana2,3 (AUTHOR), Keramatipour, Mohammad16 (AUTHOR), Casanova, Jean-Laurent2,3,17 (AUTHOR)
Source: Journal of Clinical Immunology. Nov2023, Vol. 43 Issue 8, p1941-1952. 12p.
Database: Academic Search Ultimate
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      – TitleFull: Clinical, Immunological, and Genetic Findings in Iranian Patients with MHC-II Deficiency: Confirmation of c.162delG RFXANK Founder Mutation in the Iranian Population.
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              Text: Nov2023
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