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KCNT1 Epilepsy Foundation in

KCNT1 Epilepsy Foundation

Health & Medical
 Australia

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Contact Information

Company Name
KCNT1 Epilepsy Foundation
Location

Australia

Company Details

Year Established
2019
Hours of Operation
24/7
Credentials
KCNT1, potassium ion channel, Epilepsy of Infancy with Migrating Focal Seizures (EIMFS), Early Infantile Epileptic Encephalopathy, MMPSI or Migrating Partial Epilepsy of Infancy, migrating focal seizures, Autosomal Dominant Nocturnal Frontal Lobe Epilepsy (ADNFLE) , West syndrome or Ohtahara, ion channelopathy, Coppola-Dulac Syndrome, epileptic encephalopathies of infancy, status epilepticus in infancy, EIEE14 , genetics, biogen, Ionis, ASO, antisense, “gain of function”, beyond the seizure

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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 [email protected]
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