RS2541012589 SPTAN1
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Associated Conditions
Neuronopathy
distal hereditary motor
autosomal dominant 11
Developmental delay with or without epilepsy
Neurodevelopmental abnormality
Developmental and epileptic encephalopathy
5
Neuronopathy
distal hereditary motor
autosomal dominant 11
Developmental delay with or without epilepsy
Neurodevelopmental abnormality
Developmental and epileptic encephalopathy
5
Other Variants in SPTAN1