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Results 1 - 8 of 8 for Brugada syndrome 2
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  1. SCN5A gene 
    ... of disease: current understanding and future challenges in Brugada syndrome. Nat Clin Pract Cardiovasc Med. 2005 Aug;2(8):408-14. doi: 10.1038/ncpcardio0268. Citation ...
    https://medlineplus.gov/genetics/gene/scn5a - Genetics
  2. CDKN1C gene 
    ... R, Camporeale A, Coll Vidal M, Partemi S, Brugada R, Bellocci F, Neri G. Mild Beckwith-Wiedemann and severe long-QT syndrome due to deletion of the imprinting center 2 on chromosome 11p. Eur J Hum Genet. 2013 ...
    https://medlineplus.gov/genetics/gene/cdkn1c - Genetics
  3. PRKAG2 gene 
    ... Hong K, Santana O, Brugada P, Brugada J, Brugada R. Familial pseudo-Wolff-Parkinson-White syndrome. J Cardiovasc Electrophysiol. 2006 Jul;17(7):724-32. doi: 10.1111/j.1540-8167.2006.00485.x. Citation on PubMed
    https://medlineplus.gov/genetics/gene/prkag2 - Genetics
  4. KCNH2 gene 
    ... on PubMed Hong K, Bjerregaard P, Gussak I, Brugada R. Short QT ... BP. Mechanistic basis for type 2 long QT syndrome caused by KCNH2 mutations that ...
    https://medlineplus.gov/genetics/gene/kcnh2 - Genetics
  5. CACNA1C gene 
    ... This Health Condition MedlinePlus Genetics provides information about Brugada syndrome More About This Health Condition Variants in the ... of the gene than those that cause Timothy syndrome. While these CACNA1C gene variants alter CaV1.2 channels and calcium channel flow, it is unclear ...
    https://medlineplus.gov/genetics/gene/cacna1c - Genetics
  6. HCN4 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Brugada syndrome More About This Health Condition MedlinePlus Genetics provides ...
    https://medlineplus.gov/genetics/gene/hcn4 - Genetics
  7. TRPM4 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Brugada syndrome More About This Health Condition calcium-activated non- ...
    https://medlineplus.gov/genetics/gene/trpm4 - Genetics
  8. KCNQ1 gene 
    ... Enfante E, Brugada P, Sachse F, Sanguinetti MC, Brugada R. De novo KCNQ1 mutation responsible for atrial fibrillation and short QT syndrome in utero. Cardiovasc Res. 2005 Dec 1;68( ...
    https://medlineplus.gov/genetics/gene/kcnq1 - Genetics