Low prevalence of lecithin retinol acyltransferase mutations in patients with Leber congenital amaurosis and autosomal recessive retinitis pigmentosa.
Low prevalence of lecithin retinol acyltransferase mutations in patients with Leber congenital amaurosis and autosomal recessive retinitis pigmentosa.
复制标题
莱伯先天性黑蒙和常染色体隐性遗传色素性视网膜炎患者中卵磷脂视黄醇酰基转移酶突变的患病率较低。
作者：
Sweeney,MeredithO;McGee,TerriL;Berson,EliotL;Dryja,ThaddeusP
