✦ LIBER ✦

Clinical and electrophysiological characterization of a novel mutation R863X in HERG C-terminus associated with long QT syndrome

✍ Scribed by Siyong Teng; Lijuan Ma; Yingxue Dong; Chunxia Lin; Jue Ye; Robert Bähring; Vitya Vardanyan; Yanzong Yang; Zhihu Lin; Olaf Pongs; Rutai Hui

Publisher: Springer
Year: 2004
Tongue: English
Weight: 306 KB
Volume: 82
Category: Article
ISSN: 0946-2716
DOI: 10.1007/s00109-003-0504-1

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A novel splice mutation of HERG in a Chi

A novel splice mutation of HERG in a Chinese family with long QT syndrome

✍ Shang Yun-peng; Xie Xu-dong; Wang Xing-xiang; Chen Jun-zhu; Zhu Jian-hua; Tao Qi 📂 Article 📅 2005 🏛 SP Zhejiang University Press 🌐 English ⚖ 671 KB

Novel missense mutation (G601S) of HERG

Novel missense mutation (G601S) of HERG in a Japanese long QT syndrome family

✍ Kaoru Akimoto; Michiko Furutani; Shin-Ichiro Imamura; Yoshiyuki Furutani; Hirosh 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 227 KB

A novel long-QT 5 gene mutation in the C

A novel long-QT 5 gene mutation in the C-terminus (V109I) is associated with a mild phenotype

✍ Eric Schulze-Bahr; Martin Schwarz; Susanne Hoffmann; Horst Wedekind; Harald Funk 📂 Article 📅 2001 🏛 Springer 🌐 English ⚖ 107 KB

Analysis of the human KCNH2(HERG) gene:

Analysis of the human KCNH2(HERG) gene: Identification and characterization of a novel mutation Y667X associated with long QT syndrome and a non-pathological 9 bp insertion

✍ Aimée Paulussen; Ping Yang; Menelas Pangalos; Peter Verhasselt; Roger Marrannes; 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 30 KB 👁 2 views

Long QT (LQT) syndrome is a potentially life-threatening disorder, characterized by a distinct cardiac arrhythmia known as torsades de pointes. Mutations within a number of genes linked to the familial form, including that coding for a cardiac potassium channel called KCNH2 (HERG), have been describ

New missense mutation (G626V) in the pre

New missense mutation (G626V) in the predicted selectivity filter of the HERG channel associated with familial long QT syndrome

✍ Sabine Jahr; Thorsten Lewalter; Rolf-Dieter Hesch; Berndt Lüderitz; Sabine Engli 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 10 KB 👁 1 views

Erratum to: A novel long-QT 5 gene mutat

Erratum to: A novel long-QT 5 gene mutation in the C-terminus (V109I) is associated with a mild phenotype

✍ Eric Schulze-Bahr; Martin Schwarz; Susan Hauenschild; Horst Wedekind; Harald Fun 📂 Article 📅 2001 🏛 Springer 🌐 English ⚖ 9 KB