QT Interval Determinant: Mutations, Rare Variants, or Single-Nucleotide Polymorphisms?

Circ Cardiovasc Genet. 2017 Oct;10(5):e001945. doi: 10.1161/CIRCGENETICS.117.001945.
No abstract available

Keywords: Editorials; genome-wide association study; long QT syndrome; mutation; polymorphism, single nucleotide.

Publication types

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

MeSH terms

  • Humans
  • Long QT Syndrome*
  • Mutation
  • Nucleotides
  • Polymorphism, Single Nucleotide*

Substances

  • Nucleotides