RS2538640589 GRIN1
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Associated Conditions
Neurodevelopmental disorder with or without hyperkinetic movements and seizures
autosomal recessive
autosomal dominant
Developmental and epileptic encephalopathy 101
Neurodevelopmental disorder with or without hyperkinetic movements and seizures
autosomal recessive
autosomal dominant
Developmental and epileptic encephalopathy 101
Other Variants in GRIN1