Associated Papers
Human germline biallelic loss-of-function OSMR variants cause severe allergic disease.
Sharma M et al.
Medrxiv : the Preprint Server for Health Sciences, 2025
Whole Exome Sequencing to Find Candidate Variants for the Prediction of Kidney Transplantation Efficacy.
Aghamir SMK et al.
Genes, 2023
37372431 (PubMed )
Supplement: genes-14-01251-s001.zip › HGV__1.xlsx › _1
Familial primary localized cutaneous amyloidosis results from either dominant or recessive mutations in OSMR.
Wali A et al.
Acta Dermato-venereologica, 2015
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