Sodium channel gene (SCN5A) mutations in 44 index patients with Brugada syndrome: different incidences in familial and sporadic disease.

Human mutation

Volumn 21, Issue 6, 2003, Pages 651-652

  Schulze Bahr, Eric ^a   Eckardt, Lars ^a   Breithardt, Günter ^a   Seidl, Karlheinz ^a   Wichter, Thomas ^a   Wolpert, Christian ^a   Borggrefe, Martin ^a   Haverkamp, Wilhelm ^a  

^a UNIVERSITY HOSPITAL MÜNSTER   (Germany)

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;

ADOLESCENT; ADULT; AGED; ARTICLE; CHEMISTRY; FAMILY HEALTH; GENETIC SCREENING; GENETICS; GENOTYPE; HEART VENTRICLE FIBRILLATION; HUMAN; INCIDENCE; MIDDLE AGED; MUTATION; NUCLEOTIDE SEQUENCE; PATHOLOGY; PHENOTYPE; SINGLE STRAND CONFORMATION POLYMORPHISM; SYNDROME;

ADOLESCENT; ADULT; AGED; DNA; DNA MUTATIONAL ANALYSIS; FAMILY HEALTH; GENETIC SCREENING; GENOTYPE; HUMANS; INCIDENCE; MIDDLE AGED; MUTATION; PHENOTYPE; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; SODIUM CHANNELS; SYNDROME; VENTRICULAR FIBRILLATION;

EID: 1442356568     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.9144     Document Type: Article

References (0)