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Paper Details

IFIH1 loss-of-function variants contribute to very early-onset inflammatory bowel disease.
Hum Genet
18
2021
Complete and partial MDA5 deficiency, Genetic defects of innate immunity, IBD, IBD-like enteropathy, IFIH1, IFIH1 gene, IFIH1 variants, Inflammatory Bowel Disease, Luciferase reporter, MDA5, VEOIBD, children, gastrointestinal, immunodeficiency, inflammatory bowel disease, patients, viral nucleic
Author NameAffiliation
Jennifer E PoseyBaylor College of Medicine
Shalini N JhangianiBaylor College of Medicine
James R LupskiBaylor College of Medicine
James R LupskiTexas Children's Hospital
James R LupskiBaylor College of Medicine
James R LupskiBaylor College of Medicine
James R LupskiBaylor College of Medicine
James R LupskiBaylor College of Medicine
James R LupskiBaylor College of Medicine
James R LupskiTexas Children's Hospital
Alessandra BiffiUniversity Hospital of Padova
David ValleJohns Hopkins University School of Medicine
Nara SobreiraJohns Hopkins University School of Medicine
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