The spectrum of CHM gene mutations in choroideremia and their relationship to clinical phenotype

Purpose: We report the underlying genotype and explore possible genotypic-phenotypic correlations in a large cohort of choroideremia patients. Methods: We studied prospectively a cohort of 79 patients diagnosed within a tertiary referral service for patients with retinal dystrophies. Phenotypic eval...

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Những tác giả chính: Simunovic, M, Jolly, J, Xue, K, Edwards, T, Groppe, M, Downes, S, MacLaren, R
Định dạng: Journal article
Ngôn ngữ:English
Được phát hành: Association for Research in Vision and Ophthalmology 2016