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Sa2008 - Mutations in Stxbp3 Contribute to Very Early Onset of IBD Immunodeficieny and Hearing Loss
UploadHuman TGF-β1 deficiency causes severe inflammatory bowel disease and encephalopathy
UploadGenetic and Structural Analysis of a SKIV2L Mutation Causing Tricho-hepato-enteric Syndrome
Upload25 Mutations in Stxbp3 Contribute to Very Early Onset of Ibd, Immunodeficiency and Hearing Loss
Download from academic.oup.comEnhanced TH17 Responses in Patients with IL10 Receptor Deficiency and Infantile-onset IBD:
UploadCD55 Deficiency, Early-Onset Protein-Losing Enteropathy, and Thrombosis
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