A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy
Year: 1999
Type: article
Source: Brain
Author: S. M. Zuberi
Institution: Royal Hospital for Children
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2128988164
