Phenotypic Spectrum of HCN4 Mutations: A Clinical Case

Circ Genom Precis Med. 2018 Feb;11(2):e002033. doi: 10.1161/CIRCGEN.117.002033.
No abstract available

Publication types

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

MeSH terms

  • Adult
  • Humans
  • Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels* / genetics
  • Male
  • Mood Disorders / genetics*
  • Muscle Proteins* / genetics
  • Mutation
  • Phenotype
  • Potassium Channels* / genetics
  • Sick Sinus Syndrome* / genetics
  • Ventricular Fibrillation* / genetics

Substances

  • HCN4 protein, human
  • Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels
  • Muscle Proteins
  • Potassium Channels