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Genomic organization and mutational analysis ofHERG, a gene responsible for familial long QT syndrome

โœ Scribed by Toshio Itoh; T. Tanaka; Ryozo Nagai; Tetsuro Kamiya; Toshitami Sawayama; Toshio Nakayama; Hitonobu Tomoike; Harumizu Sakurada; Yoshio Yazaki; Yusuke Nakamura


Book ID
106136931
Publisher
Springer
Year
1998
Tongue
English
Weight
180 KB
Volume
102
Category
Article
ISSN
0340-6717

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๐Ÿ“œ SIMILAR VOLUMES


Mutations at KCNQ1 and an unknown locus
โœ Kim M. Summers; Nilesh J. Bokil; Foong Teng Lu; Jiun Tsuen Low; John M. Baisden; ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 241 KB

## Abstract A large Australian family affected with long QT syndrome (LQTS) was studied. The medical characteristics of the 16 clinically affected members were consistent with LQT1. A previously identified mutation in __KCNQ1__ was found in 12 affected individuals and 1 unaffected infant but absent