A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy.
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A. Spauschus | D. Kullmann | J. Tolmie | N. Wood | R. de Silva | M. Hanna | S. Zuberi | J. Stephenson | L. Eunson | R. Mcwilliam | R. D. Silva