Brugada syndrome and abnormal splicing of SCN5A in myotonic dystrophy type 1

Archives of Cardiovascular Diseases

Volumn 106, Issue 12, 2013, Pages 635-643

  Wahbi, Karim ^a,b   Algalarrondo, Vincent ^c,d   Bécane, Henri Marc ^b   Fressart, Véronique ^e   Beldjord, Chérif ^f   Azibi, Kamel ^f   Lazarus, Arnaud ^a,g   Berber, Nawal ^b   Radvanyi Hoffman, Hélène ^h   Stojkovic, Tanya ^b   Béhin, Anthony ^b   Laforêt, Pascal ^b   Eymard, Bruno ^b   Hatem, Stéphane ^d   Duboc, Denis ^a,b  

^a UNIVERSITÉ PARIS DESCARTES   (France)

^b SORBONNE UNIVERSITÉ   (France)

^c HÔPITAL ANTOINE BÉCLÈRE   (France)

^d Sorbonne Universités   (France)

^e PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^f Institut Cochin   (France)

^g InParys Clinical Research Group   (France)

^h HÔPITAL AMBROISE PARÉ   (France)

Author keywords

Alternative splicing; Brugada syndrome; Cardiac sodium channel Na(v)1.5; Human; Myotonic dystrophy type 1; SCN5A

Indexed keywords

SODIUM CHANNEL NAV1.5;

ADULT; ALTERNATIVE RNA SPLICING; ARTICLE; BRUGADA SYNDROME; CARDIAC PATIENT; CLINICAL TRIAL; CONGESTIVE CARDIOMYOPATHY; CONTROLLED STUDY; DNA FLANKING REGION; ECG ABNORMALITY; ECHOCARDIOGRAPHY; ELECTROCARDIOGRAM; EXON; FEMALE; GENE SEQUENCE; HEART RATE; HEART TRANSPLANTATION; HEART VENTRICLE FIBRILLATION; HEART VENTRICLE TACHYCARDIA; HUMAN; HUMAN TISSUE; IMPLANTABLE CARDIOVERTER DEFIBRILLATOR; IMPLANTED HEART PACEMAKER; MAJOR CLINICAL STUDY; MALE; MYOTONIC DYSTROPHY; NUCLEOTIDE SEQUENCE; PREVALENCE; RESTRICTION MAPPING; RISK; RNA SPLICING; SUDDEN CARDIAC DEATH; TIME OF DEATH;

ALTERNATIVE SPLICING; BRUGADA SYNDROME; CANAL SODIQUE CARDIAQUE HUMAIN NA(V)1.5; CARDIAC SODIUM CHANNEL NA(V)1.5; CDNA; COMPLEMENTARY DEOXYRIBONUCLEIC ACID; DEOXYRIBONUCLEIC ACID; DM1; DMPK; DNA; DYSTROPHIA MYOTONICA PROTEIN KINASE; DYSTROPHIA MYOTONICA TYPE 1; DYSTROPHIE MYOTONIQUE DE TYPE 1; ECG; ELECTROCARDIOGRAM; ÉPISSAGE ALTERNATIF; HUMAN; MESSENGER RIBONUCLEIC ACID; MRNA; MYOTONIC DYSTROPHY TYPE 1; PCR; POLYMERASE CHAIN REACTION; REVERSE TRANSCRIPTASE; RIBONUCLEIC ACID; RNA; RT; SCN5A; SD; STANDARD DEVIATION; SYNDROME DE BRUGADA;

ADULT; ALTERNATIVE SPLICING; BIOPSY; BRUGADA SYNDROME; CASE-CONTROL STUDIES; DEATH, SUDDEN, CARDIAC; DNA MUTATIONAL ANALYSIS; ELECTROCARDIOGRAPHY; EXONS; FRANCE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MIDDLE AGED; MYOTONIC DYSTROPHY; NAV1.5 VOLTAGE-GATED SODIUM CHANNEL; PHENOTYPE; PREVALENCE; REGISTRIES; RISK FACTORS; YOUNG ADULT;

EID: 84889887414     PISSN: 18752136     EISSN: 18752128     Source Type: Journal    
DOI: 10.1016/j.acvd.2013.08.003     Document Type: Article

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