Referenced in: none

Automatically associated channels: Kv1.1

Title: Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1.

Authors: D L Browne, S T Gancher, J G Nutt, E R Brunt, E A Smith, P Kramer, M Litt

Journal, date & volume: Nat. Genet., 1994 Oct , 8, 136-40

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/7842011

Abstract