KCNT1 Epilepsy Foundation

Kcnt1 epilepsy foundation email format

Verified email-pattern data for Kcnt1 Epilepsy Foundation is currently limited. You can still use the company insights and contact sections below.
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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