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KCNT1 Epilepsy Foundation

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.

Australia

Opening Hours: 24/7

Keywords : 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,

Year : 2019

Facebook : https://m.facebook.com/kcnt1epilepsy

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Zenbu ID 1286147, since 24/09/2020
Last edited 24/09/2020 by kcnt1epilepsy
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Suburb : Ghan
Post Code : 0872

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