Referenced in: none

Automatically associated channels: Cav2.2

Title: The first disease connection for Cav2.2 channels.

Authors: Norbert Weiss

Journal, date & volume: Gen. Physiol. Biophys., 2015 Jul , 34, 217-9

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/26218636

Abstract
Commentary to: CACNA1B mutation is linked to unique myoclonus-dystonia syndrome. (Hum. Mol. Genet. 2015, pp. 987-993).