Work

Mutation in IRF2BP2 is responsible for a familial form of common variable immunodeficiency disorder

Year: 2016

Type: article

Source: Journal of Allergy and Clinical Immunology

DOI: 10.1016/j.jaci.2016.01.018

Authors: Michael D. Keller, Rahul Pandey, Dong Li, Joseph Glessner, Lifeng Tian, Sarah E. Henrickson, Ivan K. Chinn, Linda Monaco-Shawver, Jennifer Heimall, Cuiping Hou, Frederick G. Otieno, Soma Jyonouchi, Leonard Calabrese, Joris van Montfrans, Jordan S. Orange, Hakon Hakonarson

Institutions: Children's National, Children's Hospital of Philadelphia, Baylor College of Medicine, Texas Children's Hospital, Cleveland Clinic, University Medical Center Utrecht, Wilhelmina Children's Hospital

Language: English

Topic: Immunodeficiency and Autoimmune Disorders

Subfield: Immunology

Field: Immunology and Microbiology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: bronze

Funders: National Human Genome Research Institute, National Institute of Allergy and Infectious Diseases, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: Integrative Analysis of a GWAS Repository with EMRs from over 40,000 Children, The Future of Genomics Medicine in Patient Care: Contributions from CHOP, Child Health Research Career Development Award (CHRCDA) Program at Children's National, Genetic, Immunologic and Mechanistic Basis of Human NK Cell Deficiency

OpenAlex ID: W2310890057

FWCI: 3.028

Cites: 30

Cited by: 76

Related to: 10