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Novel mutations of RPGR in Chinese families with X-linked retinitis pigmentosa
BACKGROUND: RP (retinitis pigmentosa) is a group of hereditary retinal degenerative diseases. XLRP is a relatively severe subtype of RP. Thus, it is necessary to identify genes and mutations in patients who present with X-linked retinitis pigmentosa. METHODS: Genomic DNA was extracted from periphera...
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| Vydáno v: | BMC Ophthalmol |
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| Hlavní autoři: | , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2019
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6882249/ https://ncbi.nlm.nih.gov/pubmed/31775781 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12886-019-1250-7 |
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