Even pore-localizing missense variants at highly conserved sites in KCNQ1 -encoded K v 7.1 channels may have wild-type function and not cause type 1 long QT syndrome: Do not rely solely on the genetic test company's interpretation.
HeartRhythm Case Reports（2018）
关键词
Arrhythmia,Cardiac arrest,Genetics,Long QT syndrome,Pediatrics
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