[The gene defect for Finnish hereditary amyloidosis has been found]

Duodecim. 1991;107(16):1344-5.
[Article in Finnish]
No abstract available

Publication types

  • Editorial
  • Review

MeSH terms

  • Amyloidosis / genetics*
  • Chromosome Aberrations
  • Chromosome Disorders
  • Finnland
  • Gelsolin / genetics*
  • Genes, Dominant
  • Humans
  • Mutation

Substances

  • Gelsolin