Cernunnos defect in an Iranian patient with T − B + <scp>NK</scp> + severe combined immunodeficiency: A case report and review of the literature-Reference-Cited by-同舟云学术

Cernunnos defect in an Iranian patient with T ⁻ B ⁺ NK ⁺ severe combined immunodeficiency: A case report and review of the literature

Published:2022-06-02 Issue:8 Volume:10 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Molec Gen & Gen Med

Author:

Jamee Mahnaz¹²^ORCID,Khakbazan Fard Nasrin²,Fallah Shahrzad²,Golchehre Zahra³,Fallahi Mazdak²,Shamsian Bibi Shahin⁴,Sharafian Samin²,Chavoshzadeh Zahra²

Affiliation:

1. Pediatric Nephrology Research Center Research Institute for Children’s Health Shahid Beheshti University of Medical Sciences Tehran Iran

2. Immunology and Allergy Department Mofid Children's Hospital Shahid Beheshti University of Medical Sciences Tehran Iran

3. Department of Medical Genetics School of Medicine Tehran University of Medical Sciences Tehran Iran

4. Pediatric Congenital Hematologic Disorders Research Center Research Institute for Children’s Health Shahid Beheshti University of Medical Sciences Tehran Iran

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1990

Reference35 articles.

1. XLF Interacts with the XRCC4-DNA Ligase IV Complex to Promote DNA Nonhomologous End-Joining

2. Combined immunodeficiencies: twenty years experience from a single center in Turkey

3. Combined Immunodeficiency, Hemolytic Anemia, and Growth Retardation Secondary to a Homozygous Mutation in the NHEJ1 Gene

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