Genetic and functional characterisation of the P/Q calcium channel in episodic ataxia with epilepsy

CACNA1A gene non-synonymous single nucleotide polymorphisms and common migraine in Italy: a case-control association study with a micro-array technology

(2009) Stefano Gerola et al.   CLINICAL CHEMISTRY AND LABORATORY MEDICINE

Large scale calcium channel gene rearrangements in episodic ataxia and hemiplegic migraine: implications for diagnostic testing

(2009) R W Labrum et al.   JOURNAL OF MEDICAL GENETICS

Late-onset episodic ataxia type 2 associated with a novel loss-of-function mutation in the CACNA1A gene

(2009) Ester Cuenca-León et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Identification of CACNA1A large deletions in four patients with episodic ataxia

(2009) Florence Riant et al.   NEUROGENETICS

The interplay of two single nucleotide polymorphisms in the CACNA1A gene may contribute to migraine susceptibility

(2009) Mara D’Onofrio et al.   NEUROSCIENCE LETTERS

Large CACNA1A Deletion in a Family With Episodic Ataxia Type 2

(2008) Florence Riant et al.   ARCHIVES OF NEUROLOGY

Genetic Analysis of 27 Spanish Patients with Hemiplegic Migraine, Basilar-Type Migraine and Childhood Periodic Syndromes

(2008) E Cuenca-León et al.   CEPHALALGIA

Two novel alleles of tottering with distinct Ca(v)2.1 calcium channel neuropathologies

(2008) T. Miki et al.   NEUROSCIENCE

Stepwise Developmental Regression Associated With Novel CACNA1A Mutation

(2008) Andrea A. Guerin et al.   PEDIATRIC NEUROLOGY