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The KCNT1 Epilepsy Foundation U.S. based non-profit organization created by parents of children diagnosed with KCNT1 gene mutation. Our vision is to create a community of parents, researchers and supporters of those affected by KCNT1-related epilepsies.

KCNT1 Epilepsy Foundation [edit]

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http://www.kcnt1epilepsy.org

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Updated by: kcnt1epilepsy at 2020-09-24 22:19:41 UTC
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