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Volumn 64, Issue 8, 2014, Pages 745-756

HCN4 mutations in multiple families with bradycardia and left ventricular noncompaction cardiomyopathy

Author keywords

exome sequencing; genetics; HCN4; ion channel; left ventricular noncompaction cardiomyopathy; sinus bradycardia

Indexed keywords

ADOLESCENT; ADULT; AMINO ACID SUBSTITUTION; ARTICLE; ATRIOVENTRICULAR BLOCK; CARDIOVERSION; CLINICAL ARTICLE; DOPPLER ECHOCARDIOGRAPHY; ELECTROCARDIOGRAPHY; EXOME; FAMILY HISTORY; FEMALE; GENE IDENTIFICATION; GENE MUTATION; GENE SEGREGATION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC SCREENING; GENETIC VARIABILITY; HAPLOTYPE; HEART ATRIUM FIBRILLATION; HUMAN; LINKAGE ANALYSIS; MALE; MIDDLE AGED; MITRAL VALVE PROLAPSE; MITRAL VALVE REPAIR; MUTATIONAL ANALYSIS; PEDIGREE ANALYSIS; PHENOTYPE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; SINUS BRADYCARDIA; VENTRICULAR NONCOMPACTION; YOUNG ADULT;

EID: 84907951338     PISSN: 07351097     EISSN: 15583597     Source Type: Journal    
DOI: 10.1016/j.jacc.2014.05.045     Document Type: Article
Times cited : (156)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.