Search Ontology:
Human Disease

Brugada syndrome 3

Term ID
DOID:0110220
Synonyms
  • BRGDA3
Definition
A Brugada syndrome that has_material_basis_in heterozygous mutation in the gene encoding the alpha-1C subunit of the L-type voltage-dependent calcium channel (CACNA1C) on chromosome 12p13. https://www.ncbi.nlm.nih.gov/pubmed/17224476
References
Ontology
Human Disease   ( DOID:0110220 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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