Haploinsufficiency in combination with aging causes SCN5A-linked hereditary lenègre disease

Journal of the American College of Cardiology

Volumn 41, Issue 4, 2003, Pages 643-652

  Probst, Vincent ^a   Kyndt, Florence ^b   Potet, Franck ^b   Trochu, Jean Noel ^a   Mialet, Guy ^c   Demolombe, Sophie ^b   Schott, Jean Jacques ^b   Baró, Isabelle ^b   Escande, Denis ^b   Le Marec, Hervé ^a,b  

^a CHU de Nantes   (France)

^b INSERM   (France)

^c Centre Hospitalier de La Roche/Yon   (France)

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; SODIUM CHANNEL;

ADULT; AGE; AGED; AGING; ALLELE; ARTICLE; DISEASE CARRIER; EXON; FEMALE; GENE; GENE FUNCTION; GENE MUTATION; GENETIC DISORDER; GENETIC LINKAGE; GENOTYPE; HAPLOTYPE; HEART MUSCLE CONDUCTION DISTURBANCE; HEART MUSCLE FIBROSIS; HETEROZYGOTE; HIS BUNDLE; HUMAN; MAJOR CLINICAL STUDY; MALE; MUSCLE ATROPHY; P WAVE; PATHOPHYSIOLOGY; PHENOTYPE; PR INTERVAL; PRIORITY JOURNAL; PROGRESSIVE CARDIAC CONDUCTION DEFECT; QRS COMPLEX; RNA SPLICING; SCN5A GENE;

EID: 0037454049     PISSN: 07351097     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0735-1097(02)02864-4     Document Type: Article

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