Identification of an IGSF3 mutation in a family with congenital nasolacrimal duct obstruction.Foster J., Kapoor S., Diaz-Horta O., Singh A., Abad C., Rastogi A., Moharana R., Tekeli O., Walz K., Tekin M.Cited forINVOLVEMENT IN LCDDCategoryDisease & VariantsSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCClin. Genet. 86:589-591 (2014)Cited in2
IGSF3 mutation identified in patient with severe COPD alters cell function and motility.Schweitzer K.S., Jinawath N., Yonescu R., Ni K., Rush N., Charoensawan V., Bronova I., Berdyshev E., Leach S.M.[...], Petrache I.View abstractAnnotationIGSF3 mutation identified in patient with severe COPD alters cell function and motility.CategoriesSequences, Disease & VariantsSourceGeneRif: 3321PubMedEurope PMCJCI Insight 5:138101-138101 (2020)Mapped to1