Genotype and clinical characteristics of congenital long QT syndrome in Thailand

Por Ankavipar Saprungruang, Apichai Khongphatthanayothin, John Mauleekoonphairoj, Pharawee Wandee, Supaluck Kanjanauthai, Zahurul A. Bhuiyan, Arthur A.M. Wilde, Yong Poovorawan
Publicado em 2018-09-01

A heterozygous deletion mutation in the cardiac sodium channel gene SCN5A with loss- and gain-of-function characteristics manifests as isolated conduction disease, without signs of...

Por Sven Zumhagen, Marieke W Veldkamp, Birgit Stallmeyer, Antonius Baartscheer, Lars Eckardt, Matthias Paul, Carol Ann Remme, Zahurul A Bhuiyan, Connie R Bezzina, Eric Schulze-Bahr
Publicado em 2013-01-01