Calcium channelopathies in the central nervous system
Author:
Publisher
Elsevier BV
Subject
General Neuroscience
Reference52 articles.
1. Channelopathies: ion channel disorders of muscle as a paradigm for paroxysmal disorders of the nervous system;Ptacek;Neuromusc Disord,1997
2. Primary structure and functional expression from complementary DNA of a brain calcium channel;Mori;Nature,1991
3. Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4;Ophoff;Cell,1996
4. Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel;Zhuchenko;Nat Genet,1997
5. A gene for familial hemiplegic migraine maps to chromosome 19;Joutel;Nat Genet,1993
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