Molecular genetics of inherited retinal degenerations.

S Lindsay,C F Inglehearn,A Curtis,S Bhattacharya

CURRENT OPINION IN GENETICS & DEVELOPMENT（1992）

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摘要

There has recently been substantial progress in categorizing the vast range of human retinal degeneration phenotypes. A molecular approach has assigned chromosomal locations for approximately a dozen such diseases and has identifed four of the genes involved.

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rs,hr,ar,congential stationary night blindness,tcd,hereditary retinoschisis,autosomal recessive,oed,oregon eye disease,oat,tapetochoroidal dystrophy,aland island eye disease,rp,ocular albinism,xl,ad,csnb,autosomal dominant,yeast artificial chromosome,retinitis pigmentosa,ornithine aminotransferase,retinoschisis,x-linked,aied,oa,yac,molecular genetics

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