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searching for AP2M1 1 found (10 total)

alternate case: aP2M1

Myoclonic astatic epilepsy (852 words) [view diff] exact match in snippet view article find links to article

monogenic causes include mutations in the genes SLC6A1 (3p25.3),CHD2 (15q26.1), AP2M1 (10q23.2). Tonic-clonic seizures: seizures with repetitive sequences of