SCN5A R1193Q polymorphism associated with progressive cardiac conduction defects and long QT syndrome in a Chinese family

Journal of Medical Genetics

Volumn 45, Issue 2, 2008, Pages 127-128

  Sun, A ^a   Xu, L ^a   Wang, S ^a   Wang, K ^a   Huang, W ^b   Wang, Y ^b   Zou, Y ^a   Ge, J ^a  

^a FUDAN UNIVERSITY   (China)

^b CHINESE NATIONAL HUMAN GENOME CENTER AT SHANGHAI   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGED; BRUGADA SYNDROME; CHINESE; CLINICAL ARTICLE; DISEASE PREDISPOSITION; DNA SEQUENCE; ECHOCARDIOGRAPHY; ELECTROPHYSIOLOGY; FAMILY; FEMALE; GENE; GENETIC POLYMORPHISM; HEART MUSCLE CONDUCTION DISTURBANCE; HUMAN; LETTER; LONG QT SYNDROME; MALE; PRIORITY JOURNAL;

ARRHYTHMIAS, CARDIAC; ASIAN CONTINENTAL ANCESTRY GROUP; CHINA; ERYTHROMYCIN ETHYLSUCCINATE; FEMALE; HUMANS; LONG QT SYNDROME; MALE; MUSCLE PROTEINS; POLYMORPHISM, SINGLE NUCLEOTIDE; SODIUM CHANNELS;

EID: 39149094902     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.2007.056333     Document Type: Letter

References (9)

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