IndraLab

Statements

Mutated KCNA1 activates episodic ataxia type 1. 2 / 2

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"KCNA1 mutations cause episodic ataxia type 1 with myokymia (EA1)."

21858020

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reach

"Heterozygous mutations of KCNA1, the gene encoding potassium channel Kv1.1 subunits, cause episodic ataxia type 1 (EA1), which is characterized by paroxysmal cerebellar incoordination and interictal myokymia."

19779067

INDRA sources:

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IndraLab

Statements

Mutated KCNA1 activates episodic ataxia type 1. 2 / 2

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