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Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1
Browne, David L., Gancher, Stephen T., Nutt, John G., Brunt, Ewout R. P., Smith, Eric A., Kramer, Patricia, Litt, MichaelVolume:
8
Year:
1994
Pages:
5
DOI:
10.1038/ng1094-136
File:
PDF, 494 KB
1994