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==Archived wikipedia table== ==Types == {| class="wikitable sortable" border="1" |- ! Condition ! Channel type |- | [[Alternating hemiplegia of childhood]] | [[NaβΊ/KβΊ-ATPase]] |- | [[Bartter syndrome]] | various by type |- | [[Brugada syndrome]] | various, by type |- | [[Catecholaminergic polymorphic ventricular tachycardia]] (CPVT) | Calcium channel |- | [[Congenital hyperinsulinism]] | [[Inward-rectifier potassium ion channel]] |- | [[Cystic fibrosis]] | Chloride channel |- | [[Generalized epilepsy with febrile seizures plus|Dravet Syndrome]] | [[Sodium channel#Voltage-gated|Voltage-gated sodium channel]] |- | [[Episodic Ataxia]] | [[Voltage-gated potassium channel]] |- | [[Erythromelalgia]] | [[Sodium channel#Voltage-gated|Voltage-gated sodium channel]] |- | [[Generalized epilepsy with febrile seizures plus]] | [[Sodium channel#Voltage-gated|Voltage-gated sodium channel]] |- | [[Familial hemiplegic migraine]] | various |- | Associated with one particular disabling form of [[Fibromyalgia]]<ref name="BMC Musculoskelet Disord.">{{cite journal | vauthors = Vargas-Alarcon G, Alvarez-Leon E, Fragoso JM, Vargas A, Martinez A, Vallejo M, Martinez-Lavin M | title=A SCN9A gene-encoded dorsal root ganglia sodium channel polymorphism associated with severe fibromyalgia | journal=J Rheumatol Suppl | year=2012 | pages=13:23 | volume=19 |pmid=22348792| | doi=10.1186/1471-2474-13-23 | pmc=3310736}}</ref> | [[Sodium channel#Voltage-gated|Voltage-gated sodium channel]] |- | [[Hyperkalemic periodic paralysis]] | [[Sodium channel#Voltage-gated|Voltage-gated sodium channel]] |- | [[Hypokalemic periodic paralysis]] | [[Sodium channel#Voltage-gated|Voltage-gated sodium channel]]<br /> or<br /> [[voltage-dependent calcium channel]] ([[calciumopathy]]) |- | [[Lambert-Eaton myasthenic syndrome]] | [[Voltage-gated calcium channel]] |- | [[Long QT syndrome]]<br /> main type [[Romano-Ward syndrome]] | various, by type |- | [[Malignant hyperthermia]] | Ligand-gated calcium channel |- | [[Mucolipidosis type IV]] | Non-selective cation channel |- |- | [[Myotonia congenita]] | Voltage-dependent chloride channel |- | [[Neuromyelitis optica]] | [[Aquaporin]]-4 water channel |- | [[Neuromyotonia]] | Voltage-gated potassium channel |- | [[Nonsyndromic deafness]] | various |- | [[Paramyotonia congenita]]<br /> :(a [[periodic paralysis]]) | [[Sodium channel#Voltage-gated|Voltage-gated sodium channel]] |- | [[Retinitis pigmentosa]]<br /> :(some forms) | Ligand-gated non-specific ion channels |- | [[Short QT syndrome]] | various potassium channels suspected |- | [[Timothy syndrome]] | Voltage-dependent calcium channel |- | [[Tinnitus]] | Voltage-gated potassium channel of the KCNQ family |- | [[Seizure]] | Voltage-dependent potassium channel<ref>{{cite journal | authorlink2 = Arthur J. Moss | last =Hunter | first = JV | last2 = Moss | first2=AJ|title=Seizures and arrhythmias: Differing phenotypes of a common channelopathy? |journal=Neurology (journal)|volume=72 |issue=3 |pages=208β9 | date = Jan 2009 |pmid=19153369 |doi=10.1212/01.wnl.0000339490.98283.c5 |url=http://www.neurology.org/cgi/pmidlookup?view=long&pmid=19153369 |issn= |access-date=2009-04-30|quote= via=}}</ref><ref>{{cite journal | last =Mulley | first = SF | last2 = Scheffer | first2=IE| last3 = Petrou | last4 = Berkovic|title=Channelopathies as a genetic cause of epilepsy |journal=Current Opinion in Neurology |volume=16 |issue=2 |pages=171β6 | date = Apr 2003 |pmid=12644745 |doi=10.1097/00019052-200304000-00009 |url=http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?issn=1350-7540&volume=16&issue=2&spage=171 |issn= |access-date=2009-04-30|quote=|via=}}</ref> |- |} Voltage-dependent potassium channel <ref>{{cite journal | authorlink2 = Arthur J. Moss | last =Hunter | first = JV | last2 = Moss | first2=AJ|title=Seizures and arrhythmias: Differing phenotypes of a common channelopathy? |journal=Neurology (journal)|volume=72 |issue=3 |pages=208β9 | date = January 2009 |pmid=19153369 |doi=10.1212/01.wnl.0000339490.98283.c5 |url=http://www.neurology.org/cgi/pmidlookup?view=long&pmid=19153369 |issn= |access-date=2009-04-30}}</ref><ref>{{cite journal | last =Mulley | first = SF | last2 = Scheffer | first2=IE| last3 = Petrou | last4 = Berkovic|title=Channelopathies as a genetic cause of epilepsy |journal=Current Opinion in Neurology |volume=16 |issue=2 |pages=171β6 | date = April 2003 |pmid=12644745 |doi=10.1097/00019052-200304000-00009 |url=http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?issn=1350-7540&volume=16&issue=2&spage=171 |issn= |access-date=2009-04-30}}</ref> Source: Wikipedia ==Discussion ==
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