Cardiac conduction defects associate with mutations in SCN5A [4]

Nature Genetics

Volumn 23, Issue 1, 1999, Pages 20-21

  Probst, V ^a   Hoorntje, T M ^a   Hulsbeek, M ^a   Wilde, A A M ^a   Escande, D ^a   Mannens, M M A M ^a   Le Marec, H ^a  

^a HÔTEL DIEU   (France)

Author keywords

[No Author keywords available]

Indexed keywords

SODIUM CHANNEL;

CHROMOSOME 19Q; CHROMOSOME 3P; CLINICAL FEATURE; FIBROSIS; GENE LOCUS; GENE MUTATION; HEART BUNDLE BRANCH BLOCK; HEART MUSCLE CONDUCTION DISTURBANCE; HUMAN; LETTER; PEDIGREE; PHENOTYPE; PRIORITY JOURNAL; STOP CODON; SYMPTOMATOLOGY;

EID: 0032820865     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/12618     Document Type: Letter

References (16)