Whole-exome sequencing identifies Y1495X of SCN5A to be associated with familial conduction disease and sudden death

Scientific Reports

Volumn 4, Issue , 2014, Pages

  Tan, Zhi Ping ^a   Xie, Li ^a   Deng, Yao ^a   Chen, Jin Lan ^a   Zhang, Wei Zhi ^a   Wang, Jian ^a   Yang, Jin Fu ^a   Yang, Yi Feng ^a  

^a CENTRAL SOUTH UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

SCN5A PROTEIN, HUMAN; SODIUM; SODIUM CHANNEL NAV1.5; STOP CODON;

ADOLESCENT; ADULT; AGED; ARRHYTHMIAS, CARDIAC; CHILD; CONGENITAL MALFORMATION; EXOME; FEMALE; GENETIC PREDISPOSITION; GENETICS; HEART MUSCLE CONDUCTION SYSTEM; HUMAN; MALE; METABOLISM; MIDDLE AGED; PEDIGREE; PHENOTYPE; PRESCHOOL CHILD; STOP CODON; SUDDEN DEATH;

ADOLESCENT; ADULT; AGED; ARRHYTHMIAS, CARDIAC; CHILD; CHILD, PRESCHOOL; CODON, NONSENSE; DEATH, SUDDEN; EXOME; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HEART CONDUCTION SYSTEM; HUMANS; MALE; MIDDLE AGED; NAV1.5 VOLTAGE-GATED SODIUM CHANNEL; PEDIGREE; PHENOTYPE; SODIUM;

EID: 84904187561     PISSN: None     EISSN: 20452322     Source Type: Journal    
DOI: 10.1038/srep05616     Document Type: Article

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