A case of novel CACNA1A mutation causing type 2 episodic ataxia
- 19 January 2021
- journal article
- letter
- Published by Springer Science and Business Media LLC in Neurological Sciences
- Vol. 42 (6), 2577-2578
- https://doi.org/10.1007/s10072-021-05059-8
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Case report of novel CACNA1A gene mutation causing episodic ataxia type 2Sage Open Medical Case Reports, 2017
- Pearls & Oy-sters: Episodic ataxia type 2Neurology, 2016
- CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptomsEuropean Journal of Human Genetics, 2015
- Consensus Paper: Management of Degenerative Cerebellar DisordersThe Cerebellum, 2013
- Two Novel CACNA1A Gene Mutations Associated With Episodic Ataxia Type 2 and Interictal DystoniaArchives of Neurology, 2005