Very high frequency of the His1069Gln mutation in Polish Wilson disease patients

J Neurol. 1997 Sep;244(9):591-2. doi: 10.1007/s004150050149.
No abstract available

Publication types

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

MeSH terms

  • Adolescent
  • Adult
  • Amino Acid Substitution*
  • Hepatolenticular Degeneration / genetics*
  • Histidine*
  • Humans
  • Point Mutation*
  • Poland

Substances

  • Histidine