Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1 (Q24312199)
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Current Data About Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1
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(P1476) "Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1" (language: en)

(P2093) D L Browne
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S T Gancher
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J G Nutt
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E R Brunt
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E A Smith
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P Kramer
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M Litt
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(P356) 10.1038/NG1094-136
(P698) 7842011
(P3181) 233011
(P5875) 15357236
(P6179) 1004760432