Clinical Manifestations, Immunological Characteristics and Genetic Analysis of Patients with Hyper-Immunoglobulin M Syndrome in Iran-Reference-Cited by-同舟云学术

Clinical Manifestations, Immunological Characteristics and Genetic Analysis of Patients with Hyper-Immunoglobulin M Syndrome in Iran

Published:2019 Issue:1 Volume:180 Page:52-63
ISSN:1018-2438
Container-title:International Archives of Allergy and Immunology
language:en
Short-container-title:Int Arch Allergy Immunol

Author:

Tafakori Delbari Mitra,Cheraghi Taher,Yazdani Reza,Fekrvand Saba,Delavari Samaneh,Azizi Gholamreza,Chavoshzadeh Zahra,Mahdaviani Seyed Alireza,Ahanchian Hamid,Khoshkhui Maryam,Behmanesh Fatemeh,Aleyasin Soheila,Esmaeilzadeh Hossein,Jabbari-Azad Farahzad ,Fallahpour Morteza,Zamani Mohammadali,Madani Seyedeh Panid,Moazzami Bobak,Habibi Sima,Rezaei Arezou,Lotfalikhani Azadeh,Movahed Masoud,Shariat Mansoureh,Kalantari Arash,Babaei Delara,Darabi Mahshid,Parvaneh Nima,Rezaei Nima,Abolhassani Hassan,Aghamohammadi Asghar

Publisher

S. Karger AG

Subject

Immunology,General Medicine,Immunology and Allergy

Reference38 articles.

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4. Revy P, Muto T, Levy Y, Geissmann F, Plebani A, Sanal O, et al. Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the Hyper-IgM syndrome (HIGM2). Cell. 2000 Sep;102(5):565–75.

5. Imai K, Slupphaug G, Lee WI, Revy P, Nonoyama S, Catalan N, et al. Human uracil-DNA glycosylase deficiency associated with profoundly impaired immunoglobulin class-switch recombination. Nat Immunol. 2003 Oct;4(10):1023–8.

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