Clinical, genetic, and electrophysiologic characteristics of a new Pas-domain HERG mutation (M124R) causing long QT syndrome

Annals of Noninvasive Electrocardiology

Volumn 10, Issue 3, 2005, Pages 334-341

  Shushi, Liat ^a   Kerem, Batsheva ^a   Goldmit, Maya ^a   Peretz, Asher ^b   Attali, Bernard ^b   Medina, Aron ^a   Towbin, Jeffrey A ^c   Kurokawa, Junko ^d   Kass, Robert S ^d   Benhorin, Jesaia ^a,e  

^a HEBREW UNIVERSITY OF JERUSALEM   (Israel)

^b TEL AVIV UNIVERSITY   (Israel)

^c BAYLOR COLLEGE OF MEDICINE   (United States)

^d Columbia University ^*  (United States)

^e BIKUR CHOLIM HOSPITAL   (Israel)

Author keywords

HERG mutation; Long QT syndrome; PAS domain

Indexed keywords

POTASSIUM CHANNEL HERG;

ADULT; AGED; ANIMAL CELL; ARTICLE; CHO CELL; CLINICAL FEATURE; ELECTROCARDIOGRAPHY; FEMALE; GENE; GENE IDENTIFICATION; GENE MUTATION; GENETIC ANALYSIS; HEART ELECTROPHYSIOLOGY; HERG GENE; HUMAN; JEW; LONG QT SYNDROME; MAJOR CLINICAL STUDY; MALE; NONHUMAN; PATCH CLAMP; PENETRANCE; PHENOTYPE; POINT MUTATION; PRIORITY JOURNAL;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; CHILD; CHILD, PRESCHOOL; ELECTROCARDIOGRAPHY; ETHER-A-GO-GO POTASSIUM CHANNELS; FEMALE; GENOTYPE; HUMANS; INFANT; ISRAEL; LONG QT SYNDROME; MALE; MIDDLE AGED; MUTATION; PEDIGREE; PHENOTYPE; POTASSIUM CHANNELS, VOLTAGE-GATED; SEQUENCE ANALYSIS;

EID: 23844489134     PISSN: 1082720X     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1542-474X.2005.00643.x     Document Type: Article

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