Literature DB >> 11520753

Rhodopsin mutations in Chinese patients with retinitis pigmentosa.

W M Chan1, K Y Yeung, C P Pang, L Baum, T C Lau, A K Kwok, D S Lam.   

Abstract

AIM: To determine the pattern of rhodopsin mutations in Chinese retinitis pigmentosa (RP) patients.
METHODS: The rhodopsin gene was examined in 101 RP patients and 190 controls from Hong Kong.
RESULTS: Three coding changes were identified: Pro347Leu, Ala299Ser, and 5211delC. Each protein sequence alteration was found in one patient. Ala299Ser also existed in two controls.
CONCLUSION: The C-terminal nonsense mutation may cause mis-sorting of rhodopsin protein. The finding of controls with Ala299Ser suggests this is only the third missense alteration reported that does not cause RP. The expected frequency of rhodopsin mutations in RP is <7% (2/101=2.0%, 95% confidence interval: 0.2%-7.0%).

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Year:  2001        PMID: 11520753      PMCID: PMC1724134          DOI: 10.1136/bjo.85.9.1046

Source DB:  PubMed          Journal:  Br J Ophthalmol        ISSN: 0007-1161            Impact factor:   4.638


  27 in total

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