OBO ID: DOID:0111003 |
Term Name: | Joubert syndrome 8 | Search Ontology: | |
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Synonyms: |
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Definition: | A Joubert syndrome that has_material_basis_in mutation in the ARL13B gene on chromosome 3q11.1-q11.2. https://www.ncbi.nlm.nih.gov/pubmed/18674751 | ||
References: | |||
Ontology: | Human Disease ( DOID:0111003 ) |
OTHER Joubert syndrome 8 PAGES
ZEBRAFISH MODELS
Fish | Conditions | Citations |
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arl13bhi459Tg/hi459Tg | standard conditions | Zhu et al., 2020 |
PHENOTYPE
No data available
CITATIONS (1)
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