OBO ID: DOID:0080278 |
Term Name: | Joubert syndrome 32 | Search Ontology: | |
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Definition: | A Joubert syndrome that has_material_basis_in homozygous mutation in the SUFU gene on chromosome 10q24. https://pubmed.ncbi.nlm.nih.gov/28965847/ | ||
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Ontology: | Human Disease ( DOID:0080278 ) |
OTHER Joubert syndrome 32 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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