OBO ID: DOID:0060754 |
Term Name: | familial temporal lobe epilepsy 8 | Search Ontology: | |
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Definition: | A temporal lobe epilepsy characterized by autosomal dominant inheritance of complex partial seizures with occasional secondary generalization and that has_material_basis_in heterozygous mutation in the GAL gene on chromosome 11q13. https://www.ncbi.nlm.nih.gov/pubmed/25691535 | ||
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Ontology: | Human Disease ( DOID:0060754 ) |
OTHER familial temporal lobe epilepsy 8 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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