OBO ID: DOID:0060751 |
Term Name: | familial temporal lobe epilepsy 7 | Search Ontology: | |
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Definition: | A temporal lobe epilepsy characterized by autosomal dominant inheritance of focal seizures with prominent auditory symptoms and that has_material_basis_in heterozygous mutation in the RELN gene on chromosome 7q22. https://www.ncbi.nlm.nih.gov/pubmed/26046367 | ||
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Ontology: | Human Disease ( DOID:0060751 ) |
OTHER familial temporal lobe epilepsy 7 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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