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   

  文献评价指标  
  下载次数:0次 浏览次数:2次