✦ LIBER ✦

Novel mutation in the KCNH2 gene associated with long QT syndrome

✍ Scribed by Silva, Doroteia; Miltenberger-Miltenyi, Gabriel; Correia, Maria José; Diogo, António Nunes

Book ID: 122386034
Publisher: Elsevier
Year: 2013
Weight: 796 KB
Volume: 32
Category: Article
ISSN: 2174-2049
DOI: 10.1016/j.repce.2013.02.008

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Novel mutation in the KCNH2 gene associa

Novel mutation in the KCNH2 gene associated with long QT syndrome

✍ Silva, Doroteia; Miltenberger-Miltenyi, Gabriel; Correia, Maria José; Diogo, Ant 📂 Article 📅 2013 🏛 Elsevier 🌐 Portuguese ⚖ 829 KB

Novel mutation (H402R) in the S1 domain

Novel mutation (H402R) in the S1 domain of KCNH2-encoded gene associated with long QT syndrome in a Spanish family

✍ José J. Zamorano-León; Sergio Alonso-Orgaz; Javier Moreno; Rafael Cinza; Maria J 📂 Article 📅 2010 🏛 Elsevier Science 🌐 English ⚖ 137 KB

Congenital long QT syndrome with compoun

Congenital long QT syndrome with compound mutations in the KCNH2 gene

✍ Bando, Sachiko; Soeki, Takeshi; Matsuura, Tomomi; Niki, Toshiyuki; Ise, Takayuki 📂 Article 📅 2013 🏛 Springer 🌐 English ⚖ 613 KB

Functional assessment of compound mutati

Functional assessment of compound mutations in the KCNQ1 and KCNH2 genes associated with long QT syndrome

✍ Grunnet, Morten; Behr, Elijah Raphael; Calloe, Kirstine; Hofman-Bang, Jacob; Til 📂 Article 📅 2005 🏛 Elsevier Science 🌐 English ⚖ 823 KB

KCNQ1 and KCNH2 mutations associated wit

KCNQ1 and KCNH2 mutations associated with long QT syndrome in a Chinese population

✍ Wenling Liu; Junguo Yang; Dayi Hu; Cailian Kang; Cuilan Li; Shuoyan Zhang; Ping 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 285 KB

The long QT syndrome (LQTS) is a cardiac disorder characterized by prolongation of the QT interval on electrocardiograms (ECGs), syncope and sudden death caused by a specific ventricular tachyarrhythmia known as torsade de pointes. LQTS is caused by mutations in ion channel genes including the cardi

A novel mutation in the transmembrane no

A novel mutation in the transmembrane nonpore region of the KCNH2 gene causes severe clinical manifestations of long QT syndrome

✍ Liu, Li; Hayashi, Kenshi; Kaneda, Tomoya; Ino, Hidekazu; Fujino, Noboru; Uchiyam 📂 Article 📅 2013 🏛 Elsevier Science 🌐 English ⚖ 751 KB