换一批Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test.
第一作者：
Jamie D,Kapplinger
第一单位：
Department of Medicine, Divisions of Cardiovascular Diseases and Pediatric Cardiology, Windland Smith Rice Sudden Death Genomics Laboratory, Mayo Clinic, Rochester, Minnesota 55905, USA.
作者：
医学主题词
青少年(Adolescent);成年人(Adult);老年人(Aged);老年人, 80以上(Aged, 80 and over);儿童(Child);儿童, 学龄前(Child, Preschool);快速延迟整流钾通道(Ether-A-Go-Go Potassium Channels);女(雌)性(Female);基因检测(Genetic Testing);人类(Humans);婴儿, 新生(Infant, Newborn);KCNQ1钾通道(KCNQ1 Potassium Channel);QT延长综合征(Long QT Syndrome);男(雄)性(Male);中年人(Middle Aged);肌蛋白质类(Muscle Proteins);突变(Mutation);钾通道(Potassium Channels);钾通道, 电压门控(Potassium Channels, Voltage-Gated);患病率(Prevalence);回顾性研究(Retrospective Studies);危险因素(Risk Factors);钠通道(Sodium Channels);美国(United States);青年人(Young Adult)
DOI
10.1016/j.hrthm.2009.05.021
PMID
19716085
发布时间
2025-05-29
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Heart rhythm
1297-303页
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