Research - Hopkinton, New Hampshire, United States
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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