A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy.

S M Zuberi; L H Eunson; A Spauschus; R De Silva; J Tolmie; N W Wood; R C McWilliam; J B Stephenson; J P Stephenson; D M Kullmann

doi:10.1093/brain/122.5.817

A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy.

NobleID: NI8P61W49R26S43
Persistent link: https://nobleid.org/ark:/48914/w1/20260515/2D6004EC

Type:Journal Article

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A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy.

NobleID: NI8P61W49R26S43
Persistent link: https://nobleid.org/ark:/48914/w1/20260515/2D6004EC

Type:Journal Article

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