GRIN1

Glutamate receptor, ionotropic, N-methyl D-aspartate 1
2902

 

Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive – 617820

Developmental and epileptic encephalopathy 101 – 619814

Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant – 614254

 

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