RS142756900 KCNT1
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Associated Conditions
Developmental and epileptic encephalopathy
14
Autosomal dominant nocturnal frontal lobe epilepsy 5
Inborn genetic diseases
KCNT1-related disorder
Developmental and epileptic encephalopathy
14
Autosomal dominant nocturnal frontal lobe epilepsy 5
Inborn genetic diseases
KCNT1-related disorder
Other Variants in KCNT1