NEIL1 is a candidate gene associated with common variable immunodeficiency in a patient with a chromosome 15q24 deletion-Reference-Cited by-同舟云学术

NEIL1 is a candidate gene associated with common variable immunodeficiency in a patient with a chromosome 15q24 deletion

Published:2017-03 Issue: Volume:176 Page:71-76
ISSN:1521-6616
Container-title:Clinical Immunology
language:en
Short-container-title:Clinical Immunology

Author:

Romano Rosa,Zaravinos Apostolos^ORCID,Liadaki Kyriaki^ORCID,Caridha Rozina,Lundin Johanna,Carlsson Göran,Winiarski Jacek,Pan-Hammarström Qiang,Hammarström Lennart

Funder

Swedish Research Council

Publisher

Elsevier BV

Subject

Immunology,Immunology and Allergy

Reference48 articles.

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2. A large-scale survey of the novel 15q24 microdeletion syndrome in autism spectrum disorders identifies an atypical deletion that narrows the critical region;McInnes;Mol. Autism,2010

3. Characterization of a recurrent 15q24 microdeletion syndrome;Sharp;Hum. Mol. Genet.,2007

4. A further case of the recurrent 15q24 microdeletion syndrome, detected by array CGH;Klopocki;Eur. J. Pediatr.,2008

5. Myelodysplastic syndrome in a child with 15q24 deletion syndrome;Narumi;Am. J. Med. Genet. A,2012

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1. Hypogammaglobulinemia with T‐cell defects and autoimmune manifestations associated with chromosome 15q24 microdeletion;Scandinavian Journal of Immunology;2023-08-22

2. Base Excision Repair in the Immune System: Small DNA Lesions With Big Consequences;Frontiers in Immunology;2020-05-29

3. Coexistence of urogenital malformations in a female fetus with de novo 15q24 microdeletion and a literature review;Molecular Genetics & Genomic Medicine;2020-05-13

4. Refining critical regions in 15q24 microdeletion syndrome pertaining to autism;American Journal of Medical Genetics Part B: Neuropsychiatric Genetics;2020-01-18

5. Monozygotic Twins Concordant for Common Variable Immunodeficiency: Strikingly Similar Clinical and Immune Profile Associated With a Polygenic Burden;Frontiers in Immunology;2019-11-22