KCNT1 Epilepsy FoundationThe 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 Sponsored Links
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Mapped with APPROXIMATE precision
Latitude, Longitude = -25.274398, 133.775136
State :
Northern Territory
Suburb :
Ghan
Post Code :
0872
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