Homozygous familial hypercholesterolemia: A novel point mutation (W556R) in a Turkish patient

• 26 September 2000
• journal article
• case report
• Published by Hindawi Limited in Human Mutation
• Vol. 16  (4) , 374
• https://doi.org/10.1002/1098-1004(200010)16:4<374::aid-humu16>3.0.co;2-1

Abstract

Keywords

• LDL‐RECEPTOR GENE
• LDLR
• FAMILIAL HYPERCHOLESTEROLEMIA
• TURKEY