Structured Summary
Abstract
A family of delayed rectifier voltage-gated potassium channels that share homology with their founding member, KCNQ1 PROTEIN. KCNQ potassium channels have been implicated in a variety of diseases including LONG QT SYNDROME; DEAFNESS; and EPILEPSY.
MeSH Record
Classification
Broader headings
Related Concepts
Knowledge Graph
Drag nodes to rearrange; hover to trace links; click a node to open its page.
MeSH Record
Synonyms
3 entry terms
- KvLQT Potassium Channels
- Potassium Channels, KCNQ
- Potassium Channels, KvLQT
MeSH Record
Aspects Covered
30 allowable subheadings
Indexed with the subheadings administration & dosage, adverse effects, agonists, analysis, antagonists & inhibitors, biosynthesis, blood, cerebrospinal fluid, chemical synthesis, chemistry, classification, deficiency, drug effects, economics, genetics, history, immunology, isolation & purification, metabolism, pharmacokinetics, pharmacology, physiology, poisoning, radiation effects, standards, supply & distribution, therapeutic use, toxicity, ultrastructure, urine.
MeSH Record
History Note
2006(1996)
MeSH Hierarchy
Tree Numbers
AMA Style
References
- National Library of Medicine. KCNQ Potassium Channels. Medical Subject Headings (MeSH). 2026. Unique ID D051656. http://id.nlm.nih.gov/mesh/2026/D051656
- KCNQ Potassium Channels. In: Wikipedia. https://en.wikipedia.org/wiki/KCNQ_channels
- KCNQ Potassium Channels. In: Wikidata. https://www.wikidata.org/wiki/Q74805923