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Retinitis Pigmentosa: Genes and Disease Mechanisms
Retinitis pigmentosa (RP) is a group of inherited disorders affecting 1 in 3000-7000 people and characterized by abnormalities of the photoreceptors (rods and cones) or the retinal pigment epithelium of the retina which lead to progressive visual loss. RP can be inherited in an autosomal dominant, a...
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| Prif Awduron: | , , , , , |
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| Fformat: | Artigo |
| Iaith: | Inglês |
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Bentham Science Publishers Ltd.
2011
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3131731/ https://ncbi.nlm.nih.gov/pubmed/22131869 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2174/138920211795860107 |
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