The molecular basis of familial hypercholesterolaemia in Turkish patients

This publication has 40 references indexed in Scilit:

• Intronic mutations outside of Alu -repeat-rich domains of the LDL receptor gene are a cause of familial hypercholesterolemia
  Human Genetics, 2002
• The UMD-LDLR database: additions to the software and 490 new entries to the database
  Human Mutation, 2002
• The molecular basis of familial hypercholesterolemia in The Netherlands
  Human Genetics, 2001
• Genetic Localization to Chromosome 1p32 of the Third Locus for Familial Hypercholesterolemia in a Utah Kindred
  Arteriosclerosis, Thrombosis, and Vascular Biology, 2000
• Founder mutations in the LDL receptor gene contribute significantly to the familial hypercholesterolemia phenotype in the indigenous South African population of mixed ancestry
  Clinical Genetics, 1999
• Genetic testing for familial hypercholesterolaemia: practical and ethical issues
  QJM: An International Journal of Medicine, 1997
• Two novel point mutations causing receptor-negative familial hypercholesterolemia in a South African Indian homozygote
  Atherosclerosis, 1996
• Independent Mutations at Codon 3500 of the Apolipoprotein B Gene Are Associated With Hyperlipidemia
  Arteriosclerosis, Thrombosis, and Vascular Biology, 1995
• Familial ligand-defective apolipoprotein B. Identification of a new mutation that decreases LDL receptor binding affinity.
  Journal of Clinical Investigation, 1995
• Characterization of deletions in the LDL receptor gene in patients with familial hypercholesterolemia in the United Kingdom.
  Arteriosclerosis and Thrombosis: A Journal of Vascular Biology, 1992