Lindsay S, Inglehearn C F, Curtis A, Bhattacharya S
Molecular Genetics Unit Division of Human Genetics, University of Newcastle upon Tyne, UK.
Curr Opin Genet Dev. 1992 Jun;2(3):459-66. doi: 10.1016/s0959-437x(05)80158-3.
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 identified four of the genes involved.
最近,在对大量人类视网膜变性表型进行分类方面取得了重大进展。一种分子方法已确定了大约十二种此类疾病的染色体位置,并鉴定出其中四种相关基因。