OBO ID: DOID:0112232 |
Term Name: | lissencephaly 3 | Search Ontology: | |
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Definition: | A lissencephaly characterized by brain malformations, microcephaly, developmental delay and epilepsy that has_material_basis_in heterozygous mutation in the TUBA1A gene on chromosome 12q13.12. (2) | ||
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Ontology: | Human Disease ( DOID:0112232 ) |
OTHER lissencephaly 3 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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