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- W2415928018 abstract "Retinitis pigmentosa (RP) is the most common inherited eye disease that usually leads into blind, and is high simplex and clinical heterogeneity. Recent years, some new hereditary forms have been found, such as digenic RP, mitochondrial RP, incomplete dominant inheritance RP. The phenotype of RP is multiplicity. Incompatible phenomenon between genotype and phenotypes was shown in some genes such as peripherin/RDS, RHO, RP2 and RP3. The complicated phenotype was shown in the rare RP forms, such as centricity RP, stemma RP, retinitis pigmentosa sine pigmento, and retinal degeneration slow. Retinal transplantation, retinal implantation, drug and neurotrophic factor therapy, and gene therapy have been well studied worldwide and presented some hopeful efficacy. Ophthalmologists and practitioners should cognize the new advance and new knowledge on RP therapy with a scientific view for better serving the RP patients." @default.
- W2415928018 created "2016-06-24" @default.
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- W2415928018 date "2009-03-01" @default.
- W2415928018 modified "2023-09-27" @default.
- W2415928018 title "[To cognize retinitis pigmentosa with scientific view]." @default.
- W2415928018 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/19575909" @default.
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