Episodic ataxias
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Elsevier
Reference56 articles.
1. Congenital ataxia, mental retardation, and dyskinesia associated with a novel CACNA1A mutation;Blumkin;J Child Neurol,2010
2. Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1;Browne;Nat Genet,1994
3. Mutation of the Ca2+ channel beta subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (lh) mouse;Burgess;Cell,1997
4. A genome-wide screen and linkage mapping for a large pedigree with episodic ataxia;Cader;Neurology,2005
5. Late-onset episodic ataxia associated with SLC1A3 mutation;Choi;J Hum Genet.,2017
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