The Human Skeletal Muscle Na Channel Mutation R669H Associated with Hypokalemic Periodic Paralysis Enhances Slow Inactivation

Missense mutations of the human skeletal muscle voltage-gated Na channel (hSkM1) underlie a variety of diseases, including hyperkalemic periodic paralysis (HyperPP), paramyotonia congenita, and potassium-aggravated myotonia. Another disorder of sarcolemmal excitability, hypokalemic periodic paralysi...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:J Neurosci
Egile Nagusiak: Struyk, Arie F., Scoggan, Kylie A., Bulman, Dennis E., Cannon, Stephen C.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Society for Neuroscience 2000
Gaiak:
ARTICLE
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC6773093/
https://ncbi.nlm.nih.gov/pubmed/11102465
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.20-23-08610.2000
Etiketak: Etiketa erantsi
Etiketarik gabe, Izan zaitez lehena erregistro honi etiketa jartzen!

Antzeko izenburuak