Mucopolysaccharidosis type I: identification of 8 novel mutations and determination of the frequency of the two common alpha-L-iduronidase mutations (W402X and Q70X) among European patients

Hum Mol Genet. 1994 Jun;3(6):861-6. doi: 10.1093/hmg/3.6.861.

Abstract

A group of 46 European patients with mucopolysaccharidosis type I (MPS I) was screened for mutations of the alpha-L-iduronidase gene. The 2 common nonsense mutations, W402X and Q70X, were identified in, respectively, 37% and 35% of mutant alleles. Considerable differences were seen in the frequency of these 2 mutations in patients from North Europe (Norway and Finland) and other European countries (mainly The Netherlands and Germany). In Scandinavia, W402X and Q70X account for 17% and 62% of the MPS I alleles, respectively, while in other European countries W402X is about 2.5 times more frequent (48%) than Q70X (19%). Eight novel mutations are described including 4 missense mutations, 1 nonsense mutation, 1 insertion of 2 base pairs, and 2 deletions of 1 and 12 base pairs.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Amino Acid Sequence
  • Base Sequence
  • DNA Primers
  • DNA Transposable Elements
  • Europe
  • Exons
  • Finland
  • Germany
  • Humans
  • Iduronidase / genetics*
  • Molecular Sequence Data
  • Mucopolysaccharidosis I / enzymology
  • Mucopolysaccharidosis I / genetics*
  • Mutation*
  • Netherlands
  • Norway
  • Point Mutation
  • Polymerase Chain Reaction
  • Scandinavian and Nordic Countries
  • Sequence Deletion
  • Skin / enzymology
  • Skin / pathology

Substances

  • DNA Primers
  • DNA Transposable Elements
  • Iduronidase