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A molecular investigation of the novel gene underlying autosomal dominant retinitis pigmentosa in a South African family
The inherited retinal degenerative disorders are a common cause of severe visual handicap in the W estem world. Retinitis pigmentosa (RP) is a group of retinopathies in which a primary feature is a progressive loss of photoreceptor and retinal pigment epithelium function. Over the last decade, inves...
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| Format: | Thesis |
| Language: | English |
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Division of Human Genetics
2018
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