Low prevalence of lecithin retinol acyltransferase mutations in patients with Leber congenital amaurosis and autosomal recessive retinitis pigmentosa. (Q42011942)
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scientific article
Language | Label | Description | Also known as |
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English | Low prevalence of lecithin retinol acyltransferase mutations in patients with Leber congenital amaurosis and autosomal recessive retinitis pigmentosa. |
scientific article |
Statements
Low prevalence of lecithin retinol acyltransferase mutations in patients with Leber congenital amaurosis and autosomal recessive retinitis pigmentosa (English)
Meredith O Sweeney
Terri L McGee
Eliot L Berson
Thaddeus P Dryja
5 April 2007
1 reference
1 reference