Kcnt1 Epilepsy Foundation
We are parents dedicated to finding a cure for our children and all those affected by mutations in the KCNT1 gene. KCNT1 mutations can result debilitating form of epilepsy and neurological impairments caused by a gain of function problem in the potassium ion channels. We are seeking disease modifying treatments and transformational interventions for infants found to have this mutation.
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Decision-makers and verified team members
6 contacts with verified email or phone · masked until revealed.
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Ali Rosenberg
Scientific Outreach Officer · Science
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Justin West
President and Co-founder · General Business & Management
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Sarah Drislane
Executive Director · General Business & Management
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Margot Goodkin
Member Board of Directors · General Business & Management
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Top roles at Kcnt1 Epilepsy Foundation
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- 1patient advocacy intern
- 1president and co-founder
- 1scientific outreach officer
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