CACNA1H Mutations in Autism Spectrum Disorders
Open Access
- 1 August 2006
- journal article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 281 (31) , 22085-22091
- https://doi.org/10.1074/jbc.m603316200
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- A profile of alternative RNA splicing and transcript variation of CACNA1H, a human T-channel gene candidate for idiopathic generalized epilepsiesHuman Molecular Genetics, 2006
- Voltage Sensor of Kv1.2: Structural Basis of Electromechanical CouplingScience, 2005
- Functional Characterization and Neuronal Modeling of the Effects of Childhood Absence Epilepsy Variants ofCACNA1H, a T-Type Calcium ChannelJournal of Neuroscience, 2005
- Effects of Cav3.2 channel mutations linked to idiopathic generalized epilepsyAnnals of Neurology, 2005
- The Genetics of AutismPediatrics, 2004
- Postnatal Neurodevelopmental Disorders: Meeting at the Synapse?Science, 2003
- Sodium channels SCN1A, SCN2A and SCN3A in familial autismMolecular Psychiatry, 2003
- The Autism Genetic Resource Exchange: A Resource for the Study of Autism and Related Neuropsychiatric ConditionsAmerican Journal of Human Genetics, 2001
- Mutations in the hminK gene cause long QT syndrome and suppress lKs functionNature Genetics, 1997
- SLEEP AND AROUSAL: Thalamocortical MechanismsAnnual Review of Neuroscience, 1997