Prevalence, clinical significance, and genetic basis of hypertrophic cardiomyopathy with restrictive phenotype期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

Prevalence, clinical significance, and genetic basis of hypertrophic cardiomyopathy with restrictive phenotype

Authors:	Kubo Toru Gimeno Juan R Bahl Ajay Steffensen Ulla Steffensen Morten Osman Eyman Thaman Rajesh Mogensen Jens Elliott Perry M Doi Yoshinori McKenna William J

Affiliation:	^†Department of Medicine and Geriatrics, Kochi Medical School, Kochi, Japan;^‡Department of Cardiology, Skejby University Hospital, Aarhus, Denmark.;Department of Medicine, University College London, London, United Kingdom

Abstract:

Keywords:	CI, confidence interval E/A, peak E-wave/A-wave velocity ratio FS, fractional shortening HCM, hypertrophic cardiomyopathy ICD, implantable cardioverter-defibrillator LV, left ventricular LVEDD, left ventricular end-diastolic diameter LVESD, left ventricular end-systolic diameter LVH, left ventricular hypertrophy MLVWT, maximum left ventricular wall thickness MYBPC3, cardiac myosin-binding protein C gene MYH7, beta-myosin heavy chain gene RCM, restrictive cardiomyopathy R-E, Romhilt-Estes TNNI3, cardiac troponin I gene TNNT2, cardiac troponin T gene TPM1, alpha-tropomyosin gene
本文献已被 ScienceDirect PubMed 等数据库收录！