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Molecular genetic approaches to the analysis of human ophthalmic disease
D N Cooper1, M Jay, S Bhattacharya
1Haematology Department, King's College Hospital School of Medicine, Denmark Hill, London.
Eye (London, England)
|January 1, 1987
Abstract:
In this review of the recent literature, the contribution that the new techniques of molecular genetics has made in the analysis and diagnosis of human ophthalmic conditions is presented and discussed. Among the disorders reviewed are X-linked retinitis pigmentosa, Norrie's disease, gyrate atrophy and retinoblastoma, and there are also sections on crystallins and visual pigments.