Extensive Diversity of Molecular Mechanisms Underlying the Congenital Long QT Syndrome Type 1

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Bibliographic Details
Published in:Canadian journal of cardiology 2018-09, Vol.34 (9), p.1108-1109
Main Author: Horie, Minoru
Format: Article
Language:English
Subjects:
Heterozygote
Homozygote
Humans
KCNQ1 Potassium Channel - genetics
Long QT Syndrome
Phenotype
Romano-Ward Syndrome
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Online Access:Get full text
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ISSN:0828-282X
1916-7075
DOI:10.1016/j.cjca.2018.07.474