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KCN binds CACNA1A and KCNA1. 1 / 1

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"This manuscript showed that mutations in the voltage-dependent delayed rectifier potassium channel gene, KCNA1, associated with episodic ataxia cause loss, alteration and dominant-negative suppression[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"

8791523

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KCN binds CACNA1A and KCNA1. 1 / 1

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