OBO ID: DOID:0110219 |
Term Name: | Brugada syndrome 2 | Search Ontology: | |
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Definition: | A Brugada syndrome that has_material_basis_in heterozygous mutation in the GPD1L gene on chromosome 3p22. https://www.ncbi.nlm.nih.gov/pubmed/17967977 | ||
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Ontology: | Human Disease ( DOID:0110219 ) |
OTHER Brugada syndrome 2 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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