Novel AICDA mutation in a case of autosomal recessive hyper-IgM syndrome, growth hormone deficiency and autoimmunity-Reference-Cited by-同舟云学术

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Novel AICDA mutation in a case of autosomal recessive hyper-IgM syndrome, growth hormone deficiency and autoimmunity

Published:2017-01 Issue:1 Volume:45 Page:82-86
ISSN:0301-0546
Container-title:Allergologia et Immunopathologia
language:en
Short-container-title:Allergologia et Immunopathologia

Author:

Fazel A.,Kashef S.,Aleyasin S.,Harsini S.,Karamizadeh Z.,Zoghi S.,Flores S.K.,Boztug K.,Rezaei N.

Publisher

Codon Publications

Subject

General Medicine,Immunology and Allergy,Immunology,Pulmonary and Respiratory Medicine

Reference24 articles.

1. Immunoglobulin class switch recombination deficiencies;Kracker;Clin Immunol,2010

2. The hyper IgM syndrome—an evolving story;Etzioni;Pediatr Res,2004

3. Immunodeficiency mutation databases (IDbases);Piirila;Hum Mutat,2006

4. RAPID: resource of Asian primary immunodeficiency diseases;Keerthikumar;Nucleic Acids Res,2009

5. Immunoglobulin class-switch recombination deficiencies;Durandy;Arthritis Res Ther,2012

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Hyper IgM Syndrome with a Novel Mutation in the AICDA Gene: Easy to Diagnose;Asthma Allergy Immunology;2023-04-07

2. Type 2 hyper-IgM syndrome with a rare variant of AICDA gene mutation in a young woman;BMJ Case Reports;2023-03

3. Somatic hypermutation defects in two adult hyper immunoglobulin M patients;Immunologic Research;2022-07-25

4. Impact of Pituitary Autoimmunity and Genetic Disorders on Growth Hormone Deficiency in Children and Adults;International Journal of Molecular Sciences;2020-02-19

5. Protracted Diarrhea and Hypogammaglobulinemia;Pediatric Immunology;2019

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