A mouse model of episodic ataxia type-1
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Neuroscience
Link
http://www.nature.com/articles/nn1025.pdf
Reference27 articles.
1. Browne, D.L. et al. Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene KCNA1. Nat. Genet. 8, 136–140 (1994).
2. Gancher, S. & Nutt, J. Autosomal dominant episodic ataxia: a heterogeneous syndrome. Mov. Disord. 1, 239–253 (1986).
3. Brunt, E.R. & Weeden, T.W.V. Familial paroxysmal kinesigenic ataxia and continuous myokymia. Brain 113, 1361–1382 (1990).
4. Adelman, J.P., Bond, C.T., Pessia, M. & Maylie, J. Episodic ataxia results from voltage-dependent potassium channels with altered functions. Neuron 15, 1449–1454 (1995).
5. Maylie, B., Bissonnette, E., Virk, M., Adelman, J.P. & Maylie, J.G. Episodic ataxia type-1 mutations in the human Kv1.1 potassium channel alter hKvβ1-induced N-type inactivation. J. Neurosci. 22, 4786–4793 (2002).
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