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5. Autosomal dominant lateral temporal epilepsy in a family exhibiting a rare heterozygous mutation and deletion in the leucine-rich glioma inactivated 1 gene. Liu J; Hu D; Zhang Z; Tang F; Yan Y; Ma Y Neurosci Lett; 2022 Jun; 782():136698. PubMed ID: 35643238 [TBL] [Abstract][Full Text] [Related]
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