Twenty-four novel mutations in Wilson disease patients of predominantly Italian origin

Genet Test. 2007 Fall;11(3):328-32. doi: 10.1089/gte.2007.0015.

Abstract

Herein we report the results of mutation analysis of the ATP7B gene in a group of 134 Wilson disease (WD) families (268 chromosomes) prevalently of Italian origin. Using the SSCP and sequencing methods we identified 71 disease-causing mutations. Twenty-four were novel, while 19 more mutations already described, were identified in new populations in this study. A known mutation G591D showed a regional distribution, since it was only detected in 38.5% of the analyzed chromosomes in WD patients originating from Apulia, a region of South Italy. Detection of new mutations in the ATP7B gene increases our capability of molecular analysis that is essential for early diagnosis and treatment of WD.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphatases / genetics
  • Cation Transport Proteins / genetics
  • Copper-Transporting ATPases
  • DNA Mutational Analysis
  • Hepatolenticular Degeneration / epidemiology
  • Hepatolenticular Degeneration / ethnology
  • Hepatolenticular Degeneration / genetics*
  • Humans
  • Italy
  • Mutation*

Substances

  • Cation Transport Proteins
  • Adenosine Triphosphatases
  • ATP7B protein, human
  • Copper-Transporting ATPases