期刊论文详细信息
HeartRhythm Case Reports | |
Even pore-localizing missense variants at highly conserved sites in KCNQ1-encoded Kv7.1 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 | |
Michael T. Zimmermann, PhD1  David J. Tester, BS2  Michael J. Ackerman, MD, PhD2  Dan Ye, MD2  Jamie D. Kapplinger, BA3  Ashley Paquin, BA3  | |
[1] Department of Biomedical Informatics, Mayo Clinic, Rochester, Minnesota;Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic Graduate School of Biomedical Sciences, Mayo Clinic, Rochester, Minnesota;Mayo Clinic School of Medicine, Mayo Clinic, Rochester, Minnesota; | |
关键词: Arrhythmia; Cardiac arrest; Genetics; Long QT syndrome; Pediatrics; | |
DOI : 10.1016/j.hrcr.2017.04.006 | |
来源: DOAJ |
【 授权许可】
Unknown