OBO ID: DOID:0110221 |
Term Name: | Brugada syndrome 4 | Search Ontology: | |
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Definition: | A Brugada syndrome that has_material_basis_in heterozygous mutation in the gene encoding the beta-2 subunit of the voltage-dependent L-type calcium channel (CACNB2) on chromosome 10p12. https://www.ncbi.nlm.nih.gov/pubmed/17224476 | ||
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Ontology: | Human Disease ( DOID:0110221 ) |
OTHER Brugada syndrome 4 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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