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A pore mutation in a novel KQT-like potassium channel gen... | ResearchHub
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A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family
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Authors
Carole Charlier
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Carole Charlier
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Stephen Ryan
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•
Mark Leppert
Published
January 1, 1998
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Journal
Nature Genetics
Topics
Biology
Neuroscience
Molecular Biology
Cardiology And Cardiovascular Medicine
Cellular And Molecular Neuroscience
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DOI
10.1038/ng0198-53
