Open AccessClinical and electrophysiological characterization of a novel mutation (F193L) in the KCNQ1 gene associated with long QT syndrome
Author(s) -
Masato Yamaguchi,
Masami Shimizu,
Hidekazu Ino,
Hidenobu Terai,
Kenshi Hayashi,
Hiroshi Mabuchi,
Naoto Hoshi,
Haruhiro Higashida
Publication year - 2003
Publication title -
clinical science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.91
H-Index - 138
eISSN - 1470-8736
pISSN - 0143-5221
DOI - 10.1042/cs1040377
Subject(s) - long qt syndrome , proband , mink , mutation , genetics , biology , electrophysiology , sudden death , gene , qt interval , phenotype , microbiology and biotechnology , medicine , neuroscience , ecology
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