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Dive into the research topics of 'Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1'. Together they form a unique fingerprint.- Sort by
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David L. Browne, Stephen T. Gancher, John G. Nutt, Ewout R.P. Brunt, Eric A. Smith, Patricia Kramer, Michael Litt
Research output: Contribution to journal › Article › peer-review