Haploinsufficiency of<i>RCBTB1</i>is associated with Coats disease and familial exudative vitreoretinopathyJeng‐Hung Wu, Ming‐Yi Chung(National Taiwan University Hospital)Human Molecular GeneticsFebruary 11, 201610.1093/hmg/ddw041Cited by 94SaveCiteExport RISWatch citationsRelated PapersExpansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1|Nature Genetics|1993|1.7kLonger GT Repeat Polymorphism in Heme Oxygenase-1 Gene Promoter Is Associated with Peripheral Artery Obstructive Disease in Patients Receiving Hemodialysis|Acta Nephrologica|2013|0