Associated Papers
Genetic investigations on singleton school aged children reveal novel variants and new candidate genes for hearing loss.
Khan H et al.
Scientific Reports, 2024
39271758 (PubMed )
Supplement: 41598_2024_71407_MOESM1_ESM.xlsx › HLMS15_het
NOX1 loss-of-function genetic variants in patients with inflammatory bowel disease.
Schwerd T et al.
Mucosal Immunology, 2018
29091079 (PubMed )
Supplement: NIHMS895460-supplement-supplement_1.pdf
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