Channelopathy: Difference between revisions
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Revision as of 07:15, May 24, 2018
Channelopathies are diseases caused by disturbed function of ion channel subunits or the proteins that regulate them. They can be genetic or acquired, generally through an autoimmune attack on the channel.
Types
- ↑ Vargas-Alarcon G, Alvarez-Leon E, Fragoso JM, et al. (2012). "A SCN9A gene-encoded dorsal root ganglia sodium channel polymorphism associated with severe fibromyalgia". J Rheumatol Suppl. 19: 13:23. doi:10.1186/1471-2474-13-23. PMC 3310736. PMID 22348792.
- ↑ Hunter JV, Moss AJ (January 2009). "Seizures and arrhythmias: Differing phenotypes of a common channelopathy?". Neurology. 72 (3): 208–9. doi:10.1212/01.wnl.0000339490.98283.c5. PMID 19153369. Retrieved April 30, 2009.
- ↑ Mulley JC, Scheffer IE, Petrou S, Berkovic SF (April 2003). "Channelopathies as a genetic cause of epilepsy". Current Opinion in Neurology. 16 (2): 171–6. doi:10.1097/00019052-200304000-00009. PMID 12644745. Retrieved April 30, 2009.