An amino acid exchange in exon I of the human lecithin:cholesterol acyltransferase (LCAT) gene is associated with Fish Eye Disease
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference17 articles.
1. FISH-EYE DISEASE A NEW FAMILIAL CONDITION WITH MASSIVE CORNEAL OPACITIES AND DYSLIPOPROTEINÆMIA
2. The isolation and characterisation of a cDNA clone for human lecithin:cholesterol acyl transferase and its use to analyse the genes in patients with LCAT deficiency and fish eye disease
3. Human lecithin-cholesterol acyltransferase gene: complete gene sequence and sites of expression
4. Skretting, G., Larsen, F., Kolstø, A.B., and Prydz, H. EMBL accession no. X5 1966.
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