Phenotypic characterization of 3 families with autosomal dominant retinitis pigmentosa due to mutations in KLHL7

Wen Y, Locke KG, Klein M, Bowne SJ, Sullivan LS, Ray JW, Daiger SP, Birch DG, Hughbanks-Wheaton DK. Phenotypic characterization of 3 families with autosomal dominant retinitis pigmentosa due to mutations in KLHL7. Arch Ophthalmol. 2011 Nov;129(11):1475-82.