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1-10 employees
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Research
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Contoocook, NH 03229 , US
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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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KCNT1 Epilepsy Foundation Email Formats | Example Email Formats | Percentage |
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{f}{last} | [email protected] |
75.00%
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The widely used KCNT1 Epilepsy Foundation email format is {f}{last} (e.g. [email protected]) with 75.00% adoption across the company.
To contact KCNT1 Epilepsy Foundation customer service number in your country click here to find.
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