Relationship between congenital long QT syndrome and Brugada syndrome gene mutation

Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae

Volumn 27, Issue 3, 2005, Pages 289-294

  Du, Rong ^a   Ren, Fa xin ^a   Yang, Jun guo ^a   Yuan, Guo hui ^a   Zhang, Shou yan ^a   Kang, Cai lian ^a   Li, Wei ^a   Gui, L ^a   Li, Jing ^a  

^a HUAZHONG UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

KCNE1 PROTEIN, HUMAN; KCNH2 PROTEIN, HUMAN; KCNQ1 PROTEIN, HUMAN; MUSCLE PROTEIN; POTASSIUM CHANNEL HERG; POTASSIUM CHANNEL KCNQ1; SCN5A PROTEIN, HUMAN; SODIUM CHANNEL; VOLTAGE GATED POTASSIUM CHANNEL;

ADOLESCENT; ADULT; ARTICLE; FEMALE; GENETICS; HUMAN; LONG QT SYNDROME; MALE; MIDDLE AGED; MOLECULAR GENETICS; MUTATION; NUCLEOTIDE SEQUENCE; PEDIGREE;

ADOLESCENT; ADULT; BASE SEQUENCE; ETHER-A-GO-GO POTASSIUM CHANNELS; FEMALE; HUMANS; JERVELL-LANGE NIELSEN SYNDROME; KCNQ1 POTASSIUM CHANNEL; LONG QT SYNDROME; MALE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; MUSCLE PROTEINS; MUTATION; PEDIGREE; POTASSIUM CHANNELS, VOLTAGE-GATED; ROMANO-WARD SYNDROME; SODIUM CHANNELS;

EID: 33645932016     PISSN: 1000503X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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