Rapid screening of the LDL receptor point mutation FH-Genoa/Palermo. Mutation in brief no. 238. Online

Hum Mutat. 1999;13(5):412. doi: 10.1002/(sici)1098-1004(1999)13:5<412::aid-humu12>3.0.co;2-q.

Abstract

The LDL-receptor gene point mutation FH-Genoa/Palermo is the most frequent mutation responsible for Familial Hypercholesterolemia in Sicily. The mutation does not introduce or abolish any useful restriction site. We establish a GeneComb-based strategy to identify this mutation in a population of Sicilian unrelated clinically diagnosed FH probands. The method was very sensitive and specific; 12 out of 90 (13.3%) unrelated FH probands were found to carry the FH-Genoa/Palermo mutation. According to these results, the FH-Genoa/Palermo is the more frequent LDL-receptor gene mutation among the Sicilian FH patients. Moreover FH-Genoa/Palermo is the mutation cluster to date more represented in Southern Italy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Genetic Testing*
  • Humans
  • Hyperlipoproteinemia Type II / genetics*
  • Point Mutation*
  • Receptors, LDL / genetics*

Substances

  • Receptors, LDL