Homozygous SCN5A mutation in long-QT syndrome with functional two-to-one atrioventricular block.

Circulation research

Volumn 89, Issue 2, 2001, Pages

  Lupoglazoff, J M ^a   Cheav, T ^a   Baroudi, G ^a   Berthet, M ^a   Denjoy, I ^a   Cauchemez, B ^a   Extramiana, F ^a   Chahine, M ^a   Guicheney, P ^a  

^a HÔPITAL ROBERT DEBRÉ   (France)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; SODIUM CHANNEL; VOLTAGE GATED NA+ CHANNEL NA(V)1.5A; VOLTAGE-GATED NA+ CHANNEL NA(V)1.5A;

AMINO ACID SEQUENCE; ARTICLE; CASE REPORT; CELL LINE; CELL MEMBRANE POTENTIAL; CHEMISTRY; FAMILY HEALTH; FEMALE; GENETICS; HAPLOTYPE; HEART BLOCK; HOMOZYGOTE; HUMAN; LONG QT SYNDROME; MALE; MISSENSE MUTATION; MUTATION; NUCLEOTIDE SEQUENCE; PATHOLOGY; PATHOPHYSIOLOGY; PEDIGREE; PHYSIOLOGY; PRESCHOOL CHILD; SEQUENCE HOMOLOGY; SINGLE STRAND CONFORMATION POLYMORPHISM;

AMINO ACID SEQUENCE; BASE SEQUENCE; CELL LINE; CHILD, PRESCHOOL; DNA; DNA MUTATIONAL ANALYSIS; FAMILY HEALTH; FEMALE; HAPLOTYPES; HEART BLOCK; HOMOZYGOTE; HUMANS; LONG QT SYNDROME; MALE; MEMBRANE POTENTIALS; MUTATION; MUTATION, MISSENSE; PEDIGREE; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; SEQUENCE HOMOLOGY, AMINO ACID; SODIUM CHANNELS;

MLCS; MLOWN;

EID: 0007519279     PISSN: None     EISSN: 15244571     Source Type: Journal    
DOI: 10.1161/hh1401.095087     Document Type: Article

References (0)