Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1 (Q24312199)

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Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1
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    Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1 (English)
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    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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    October 1994
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    8
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    136-40
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    2
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