Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1 - Concepedia

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Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1

775

Citations

18

References

1994

Year

D.L. Browne, Stephen T. Gancher, John G. Nutt, E. R. Brunt, Eric A. Smith, Patricia Kramer, M. Litt

Nature Genetics

ChannelopathiesMolecular NeuroscienceEpisodic Ataxia/myokymia SyndromePoint MutationsHyperpolarization (Biology)Genetic DisorderGeneticsNeuroscienceMedicinePotassium HomeostasisSocial SciencesNeurogenetics

References

	Year	Citations

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