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Paper Details

Mutation spectrum of NOD2 reveals recessive inheritance as a main driver of Early Onset Crohn's Disease.
Sci Rep
28
2021
CD, Crohn's Disease, Crohn's disease, IBD, IBD-unclassified, Inflammatory bowel disease, Mendelian disease gene, NOD2, NOD2 alleles, NOD2 protein, NOD2 risk alleles, NOD2 variants, UC, chronic inflammation of the gastrointestinal tract, intestinal stricturing, patients, perianal disease, ulcerative colitis
Author NameAffiliation
Cristopher V Van HoutRegeneron Pharmaceuticals Inc.
Jeffrey G ReidRegeneron Pharmaceuticals Inc.
Jeffrey G ReidRegeneron Pharmaceuticals Inc.
John D OvertonRegeneron Pharmaceuticals Inc.
John D OvertonRegeneron Pharmaceuticals Inc.
Aris BarasRegeneron Pharmaceuticals Inc.
Alan R ShuldinerRegeneron Pharmaceuticals Inc.
Alan R ShuldinerRegeneron Pharmaceuticals Inc.
Omri GottesmanRegeneron Pharmaceuticals Inc.
Omri GottesmanRegeneron Pharmaceuticals Inc.
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Release 1.2