✦ LIBER ✦

Molecular, cellular, and functional analysis of a novel long QT type 2 deletion

✍ Scribed by Lian, Jianfang; Cui, Changzong; Xue, Xiaolin; Zhang, Li; Huang, Cheng; Ma, Aiqun; Vincent, G. Michael; Anson, Blake Anson D.; January, Craig T.

Book ID: 123434603
Publisher: Elsevier Science
Year: 2005
Tongue: English
Weight: 54 KB
Volume: 2
Category: Article
ISSN: 1547-5271
DOI: 10.1016/j.hrthm.2005.02.928

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The diagnosis and molecular analysis of

The diagnosis and molecular analysis of a novel 21.9kb deletion (Qinzhou type deletion) causing α+ thalassemia

✍ Long, Ju; Yan, Shanhuo; Lao, Kegan; Pang, Wanrong; Ye, Xuehe; Sun, Lei 📂 Article 📅 2014 🏛 Elsevier Science 🌐 English ⚖ 810 KB

Novel mechanism of a C-terminal intronic

Novel mechanism of a C-terminal intronic splicing mutation in type 2 long QT syndrome

✍ Zhou, Zhengfeng; Zhang, Li; Moss, Arthur J.; Vincent, G. Michael; Tabor, Kristen 📂 Article 📅 2005 🏛 Elsevier Science 🌐 English ⚖ 52 KB

Long QT syndrome with cardiac arrest and

Long QT syndrome with cardiac arrest and transient short QT due to a novel KCNH2 mutation causing both loss and gain of function

✍ De Ferrari, Gaetano M.; Crotti, Lia; Lundquist, Andrew L.; Pedrazzini, Matteo; I 📂 Article 📅 2005 🏛 Elsevier Science 🌐 English ⚖ 77 KB

Molecular and Functional Characterizatio

Molecular and Functional Characterization of a Novel Pathogenic Substrate for Autosomal Dominant Long QT Syndrome Discovered by Whole Exome Sequencing, Genomic Triangulation, and Systems Biology

✍ Boczek, N.J.; Best, J.M.; Tester, D.J.; Giudicessi, J.R.; Kamp, T.J.; Ackerman, 📂 Article 📅 2012 🏛 Elsevier Science 🌐 English ⚖ 74 KB

Molecular cloning and functional analysi

Molecular cloning and functional analysis of a novel Cx43 partner protein CIP150

✍ Motofusa Akiyama; Norihiro Ishida; Takuya Ogawa; Keiichiro Yogo; Tatsuo Takeya 📂 Article 📅 2005 🏛 Elsevier Science 🌐 English ⚖ 576 KB

PM025 A Severe Type of Long QT Syndrome

PM025 A Severe Type of Long QT Syndrome and Cardiovascular Anomaly in a Homozygous Carrier of a Novel KCNH2 Mutation and Findings in Family Screening

✍ Al-Senaidi, Khalfan S.; Wang, Guoliang; Zhang, Li; Beer, Dominik A.; Al-Farqani, 📂 Article 📅 2014 🏛 Elsevier 🌐 English ⚖ 305 KB