Clinical, Immunological, and Genetic Findings in Iranian Patients with MHC-II Deficiency: Confirmation of c.162delG RFXANK Founder Mutation in the Iranian Population-Reference-Cited by-同舟云学术

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

Published:2023-08-16 Issue:8 Volume:43 Page:1941-1952
ISSN:0271-9142
Container-title:Journal of Clinical Immunology
language:en
Short-container-title:J Clin Immunol

Author:

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,Mahdavi Mohadese,Heydarazad Zadeh Maryam,Shokri Mehdi,Alizadeh Fatemeh,Movahedi Mahshid,Momenilandi Mana,Keramatipour Mohammad,Casanova Jean-Laurent,Cobat Aurélie,Abel Laurent,Shahrooei Mohammad,Parvaneh Nima^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Immunology,Immunology and Allergy

Link

https://link.springer.com/content/pdf/10.1007/s10875-023-01562-z.pdf

Reference55 articles.

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3. Reith W, Mach B. The bare lymphocyte syndrome and the regulation of MHC expression. Annu Rev Immunol. 2001;19:331.

4. Villard J, Masternak K, Lisowska-Grospierre B, Fischer A, Reith W. MHC class II deficiency: a disease of gene regulation. Medicine. 2001;80(6):405–18.

5. Griscelli C, Lisowska-Grospierre B, Le Deist F, Durandy A, Marcadet A, Fischer A, et al. Combined immunodeficiency with abnormal expression of MHC class II genes. Clin Immunol Immunopathol. 1989;50(1 Pt 2):S140–8.

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