Haplotype and Mutation Analysis in Greek Patients With Wilson Disease

Eur J Hum Genet. Sep-Oct 1998;6(5):487-91. doi: 10.1038/sj.ejhg.5200219.

Abstract

In this study, we report the results of haplotype and mutation analysis of the ATP7B gene in Wilson disease (WD) patients of Greek origin. We have analysed 25 WD families and two single patients and characterised 94% of the WD chromosomes investigated. We have found 12 different molecular defects (three frameshifts, two splice site, two nonsense, five missense mutations), four of which are novel. Five of the mutations are widely prevalent accounting for 74% of the WD chromosomes analysed. These results may enable preclinical diagnosis in the large majority of WD patients of Greek descent, thereby improving genetic counselling and disease management.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Base Sequence
  • Child
  • Child, Preschool
  • DNA Primers
  • Genotype
  • Greece / ethnology
  • Haplotypes*
  • Hepatolenticular Degeneration / ethnology
  • Hepatolenticular Degeneration / genetics*
  • Humans
  • Mutation
  • Polymorphism, Single-Stranded Conformational

Substances

  • DNA Primers