RPGR mutation associate with retinitis pigmentosa, impaired hearing, and sinorespiratory infections

Authors :: Zito, I
Downes, SM
Patel, RJ
Cheetham, ME
Ebenezer, ND
Jenkins, SA
Bhattacharya, SS
Webster, AR
Holder, GE
Bird, AC
Bamiou, DE
Hardcastle, AJ
Source :: Journal of Medical Genetics. August 2003, Vol. 40 Issue 8, p609, 7 p.
Publication Year :: 2003
Abstract: Retinitis pigmentosa (RP) is a progressive retinal degeneration that affects about 1 in 4000 of the population. (1) Approximately 15-30% of patients with RP have X linked retinitis pigmentosa (XLRP), [...]

Subjects :: Genetic disorders -- Research -- Genetic aspects
Human genetics -- Research -- Genetic aspects
Retinitis pigmentosa -- Genetic aspects -- Research
Health
Research
Genetic aspects

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