Referenced in: none

Automatically associated channels: Cav2.1

Title: Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a family with familial hemiplegic migraine type 1, cerebellar atrophy and mental retardation.

Authors: T Freilinger, M Bohe, B Wegener, B Müller-Myhsok, M Dichgans, H Knoblauch

Journal, date & volume: Cephalalgia, 2008 Apr , 28, 403-7

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/18279427

Abstract