Genetic analysis of erythrocytosis reveals possible causative and modifier gene mutations

Br J Haematol. 2019 Aug;186(4):e100-e103. doi: 10.1111/bjh.15931. Epub 2019 Apr 23.
No abstract available

Keywords: EGLN1/PHD2; HFE SNVs; erythrocytosis.

Publication types

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

MeSH terms

  • Alleles
  • Biomarkers
  • Genes, Modifier*
  • Genetic Association Studies / methods
  • Genetic Predisposition to Disease*
  • Genotype
  • Humans
  • Mutation*
  • Pedigree
  • Polycythemia / diagnosis
  • Polycythemia / genetics*
  • Polycythemia / metabolism

Substances

  • Biomarkers