Expanding the Phenotypic Spectrum of CACNA1H Mutations
- 18 December 2018
- journal article
- research article
- Published by Elsevier BV in Pediatric Neurology
- Vol. 93, 50-55
- https://doi.org/10.1016/j.pediatrneurol.2018.11.017
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Association study between polymorphisms in the CACNA1A, CACNA1C, and CACNA1H genes and drug-resistant epilepsy in the Chinese Han populationSeizure, 2015
- Mechanisms by which a CACNA1H mutation in epilepsy patients increases seizure susceptibilityThe Journal of Physiology, 2014
- T-type calcium channels in burst-firing, network synchrony, and epilepsyBiochimica et Biophysica Acta (BBA) - Biomembranes, 2012
- Contributions of T-type calcium channel isoforms to neuronal firingChannels, 2010
- Extended spectrum of idiopathic generalized epilepsies associated with CACNA1H functional variantsAnnals of Neurology, 2007
- The Role of T-Channels in the Generation of Thalamocortical RhythmsCNS & Neurological Disorders - Drug Targets, 2006
- CACNA1H Mutations in Autism Spectrum DisordersJournal of Biological Chemistry, 2006
- Low-Voltage-Activated (“T-Type”) Calcium Channels in ReviewJournal of Bioenergetics and Biomembranes, 2003
- Association between genetic variation of CACNA1H and childhood absence epilepsyAnnals of Neurology, 2003