Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 7 of 7 for Brugada syndrome 5
Did you mean uganda syndrome 5?
  1. KCNH2 gene 
    ... Guerchicoff A, Bianchi F, Giustetto C, Schimpf R, Brugada P, Antzelevitch C. Sudden death associated with short-QT syndrome linked to mutations in HERG. Circulation. 2004 Jan 6;109(1):30-5. doi: 10.1161/01.CIR.0000109482.92774.3A. ...
    https://medlineplus.gov/genetics/gene/kcnh2 - Genetics
  2. SCN5A gene 
    ... nocturnal death syndrome (SUNDS), a disease allelic to Brugada syndrome. Hum Mol ... gene product NaV1.5: Role in physiology and pathophysiology. Gene. 2015 Dec ...
    https://medlineplus.gov/genetics/gene/scn5a - Genetics
  3. PRKAG2 gene 
    ... Mol Cell Cardiol. 2003 Oct;35(10):1251-5. doi: 10.1016/s0022-2828(03)00237-2. Citation on PubMed Sternick EB, Oliva A, Magalhaes LP, Gerken LM, Hong K, Santana O, Brugada P, Brugada J, Brugada R. Familial pseudo-Wolff-Parkinson-White syndrome. J Cardiovasc Electrophysiol. 2006 Jul;17(7):724- ...
    https://medlineplus.gov/genetics/gene/prkag2 - Genetics
  4. 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
  5. CACNA1C gene 
    ... This Health Condition MedlinePlus Genetics provides information about Brugada syndrome More About This Health Condition Variants in the ...
    https://medlineplus.gov/genetics/gene/cacna1c - Genetics
  6. KCNQ1 gene 
    ... Loussouarn G. Impaired KCNQ1-KCNE1 and phosphatidylinositol-4,5-bisphosphate interaction underlies the long QT syndrome. Circ Res. 2005 Apr 15;96(7):730- ...
    https://medlineplus.gov/genetics/gene/kcnq1 - Genetics
  7. 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 ...
    https://medlineplus.gov/genetics/gene/cdkn1c - Genetics