Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for brugada syndrome

Human Molecular Genetics

Volumn 24, Issue 10, 2015, Pages 2757-2763

  Le Scouarnec, Solena ^a,b,c   Karakachoff, Matilde ^a,b,c,d   Gourraud, Jean Baptiste ^a,b,c   Lindenbaum, Pierre ^a,b,c   Bonnaud, Stéphanie ^a,b,c   Portero, Vincent ^a,b,c   Duboscq Bidot, Laëtitia ^a,b,c   Daumy, Xavier ^a,b,c   Simonet, Floriane ^a,b,c   Teusan, Raluca ^a,b,c   Baron, Estelle ^a,b,c   Violleau, Jade ^a,b,c   Persyn, Elodie ^a,b,c   Bellanger, Lise ^c,e   Barc, Julien ^f,g   Chatel, Stéphanie ^a,b,c   Martins, Raphaël ^h   Mabo, Philippe ^h   Sacher, Frédéric ⁱ   Haïssaguerre, Michel ⁱ   Kyndt, Florence ^a,b,c   Schmitt, Sébastien ^c,j   Bézieau, Stéphane ^c,j   Le Marec, Hervé ^a,b,c   Dina, Christian ^a,b,c   Schott, Jean Jacques ^a,b,c   Probst, Vincent ^a,b,c   Redon, Richard ^a,b,c   more..

^a L INSTITUT DU THORAX   (France)

^b CNRS   (France)

^c UNIVERSITÉ DE NANTES   (France)

^d CNR   (Italy)

^e Universite de Nantes   (France)

^f ACADEMIC MEDICAL CENTER   (Netherlands)

^g ROYAL NETHERLANDS ACADEMY OF ARTS AND SCIENCES   (Netherlands)

^h RENNES UNIVERSITY HOSPITAL   (France)

ⁱ BORDEAUX UNIVERSITY HOSPITAL   (France)

^j NANTES UNIVERSITY HOSPITAL   (France)

more..

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM CHANNEL L TYPE; PROTEIN CACNA1C; SODIUM CHANNEL NAV1.5; SODIUM CHANNEL NAV1.8; UNCLASSIFIED DRUG; SCN5A PROTEIN, HUMAN;

ADULT; AMINO ACID SEQUENCE; ARTICLE; BRUGADA SYNDROME; CONTROLLED STUDY; ECG ABNORMALITY; ELECTROCARDIOGRAM; FEMALE; GENE FREQUENCY; GENE SEQUENCE; GENETIC CONSERVATION; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; HEART ARRHYTHMIA; HIGH THROUGHPUT SEQUENCING; HUMAN; MAJOR CLINICAL STUDY; MALE; MOLECULAR DIAGNOSIS; PREVALENCE; PRIORITY JOURNAL; CAUCASIAN; DNA SEQUENCE; GENE; GENETIC ASSOCIATION; GENETIC PREDISPOSITION; GENETICS; MIDDLE AGED; MUTATION;

ADULT; ARRHYTHMIAS, CARDIAC; BRUGADA SYNDROME; EUROPEAN CONTINENTAL ANCESTRY GROUP; FEMALE; GENE FREQUENCY; GENES; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MIDDLE AGED; MUTATION; NAV1.5 VOLTAGE-GATED SODIUM CHANNEL; SEQUENCE ANALYSIS, DNA;

EID: 84929717941     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddv036     Document Type: Article

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