Haplotype analysis of newly diagnosed Portuguese and Brazilian families with fibrinogen amyloidosis caused by the FGA p.Glu545Val variant

Amyloid. 2019;26(sup1):144-145. doi: 10.1080/13506129.2019.1582500.
No abstract available

MeSH terms

  • Amino Acid Substitution
  • Amyloidosis / genetics*
  • Brazil
  • Family*
  • Female
  • Fibrinogen / genetics*
  • Haplotypes*
  • Humans
  • Male
  • Mutation, Missense*
  • Polymorphism, Genetic*
  • Portugal

Substances

  • FGA protein, human
  • Fibrinogen