The application proposes to identify genes responsible for an autosomal dominant form of idiopathic ventricular fibrillation, the Brugada Syndrome. PI is following up the identification of mutations in a cardiac sodium channel gene (SCN5A) in three families with this disorder. Other families are NOT linked to SCN5A and so the PI proposes to map them by linkage, assess candidate genes (channel protein genes) if they map to the appropriate location, do fine mapping and physical mapping and gene isolation by positional cloning and positional EST candidate approaches. If pathogenic mutations are found, he proposes to collaborate in expressing them in frog oocytes to study the effect of the mutations on ion fluxes and action potentials.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
1R01HL062570-01
Application #
2840548
Study Section
Mammalian Genetics Study Section (MGN)
Project Start
1999-04-01
Project End
2003-03-31
Budget Start
1999-04-01
Budget End
2000-03-31
Support Year
1
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Baylor College of Medicine
Department
Pediatrics
Type
Schools of Medicine
DUNS #
074615394
City
Houston
State
TX
Country
United States
Zip Code
77030
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