Common variants in the hERG (KCNH2) voltage-gated potassium channel are associated with altered fasting and glucose-stimulated plasma incretin and glucagon responses

BACKGROUND: Patients with long QT syndrome due to rare loss-of-function mutations in the human ether-á-go-go-related gene (hERG) have prolonged QT interval, risk of arrhythmias, increased secretion of insulin and incretins and impaired glucagon response to hypoglycemia. This is caused by a dysfuncti...

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Detalles Bibliográficos
Autores principales: Engelbrechtsen, Line, Mahendran, Yuvaraj, Jonsson, Anna, Gjesing, Anette Prior, Weeke, Peter E., Jørgensen, Marit E., Færch, Kristine, Witte, Daniel R., Holst, Jens J., Jørgensen, Torben, Grarup, Niels, Pedersen, Oluf, Vestergaard, Henrik, Torekov, Signe, Kanters, Jørgen K., Hansen, Torben
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5857134/
https://www.ncbi.nlm.nih.gov/pubmed/29548277
http://dx.doi.org/10.1186/s12863-018-0602-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5857134/
https://www.ncbi.nlm.nih.gov/pubmed/29548277
http://dx.doi.org/10.1186/s12863-018-0602-2

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