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Heart Rhythm

Volumn 1, Issue 1, 2004, Pages 65-66

Congenital long QT syndrome: Looking beyond the heart

(1) Rubart, Michael a,b

a INDIANA UNIVERSITY SCHOOL OF MEDICINE (United States)

b INDIANA UNIVERSITY SCHOOL OF MEDICINE (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANKYRIN; ANTIARRHYTHMIC AGENT; NEUROTRANSMITTER; POTASSIUM CHANNEL KCNQ1; PROLACTIN;

ARRHYTHMOGENESIS; AUDITORY STIMULATION; CELL MEMBRANE DEPOLARIZATION; DISEASE ASSOCIATION; EDITORIAL; EMOTIONAL STRESS; GENE MUTATION; GENETIC CODE; GENOTYPE; GENOTYPE PHENOTYPE CORRELATION; HEART ARRHYTHMIA; HUMAN; LONG QT SYNDROME; MUTATIONAL ANALYSIS; NERVE CELL EXCITABILITY; NEUROENDOCRINE DISEASE; PATHOPHYSIOLOGY; PREGNANCY; PRIORITY JOURNAL; PROBABILITY; PROLACTIN BLOOD LEVEL; PUERPERIUM; RISK ASSESSMENT; RISK FACTOR; SYMPATHETIC FUNCTION; TORSADE DES POINTES;

FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENETIC SCREENING; HEART DEFECTS, CONGENITAL; HUMANS; LONG QT SYNDROME; MUTATION; POSTPARTUM PERIOD; PREGNANCY;

EID: 2442560043 PISSN: 15475271 EISSN: None Source Type: Journal
DOI: 10.1016/j.hrthm.2004.02.008 Document Type: Editorial

Times cited : (5)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.