About
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 and support research for clinical treatments. We have a KCNT1 patient registry and want to find people affected by KCNT1 across the globe to join the registry. We can work with researchers to utilize this information to find treatments and a cure. www.KCNT1epilepsy.org or contact info@kcnt1epilepsy.org
Hours : 24/7
Year : 2019
Facebook : m.facebook.com/kcnt1epilepsy
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