NOS1AP Is a Genetic Modifier of the Long-QT Syndrome-Reference-Cited by-同舟云学术

NOS1AP Is a Genetic Modifier of the Long-QT Syndrome

Published:2009-10-27 Issue:17 Volume:120 Page:1657-1663
ISSN:0009-7322
Container-title:Circulation
language:en
Short-container-title:Circulation

Author:

Crotti Lia¹,Monti Maria Cristina¹,Insolia Roberto¹,Peljto Anna¹,Goosen Althea¹,Brink Paul A.¹,Greenberg David A.¹,Schwartz Peter J.¹,George Alfred L.¹

Affiliation:

1. From the Section of Cardiology, Department of Lung, Blood, and Heart (L.C., P.J.S.), and Department of Heath Sciences (M.C.M.), University of Pavia, Pavia, Italy; Department of Cardiology (L.C., P.J.S.) and Molecular Cardiology Laboratory (L.C., R.I., P.J.S.), IRCCS Fondazione Policlinico San Matteo, Pavia, Italy; Division of Statistical Genetics, Department of Biostatistics, Mailman School of Public Health, and Psychiatry Department, Columbia University Medical Center, New York, NY (M.C.M., D.A.G....

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Reference33 articles.

1. Schwartz PJ Crotti L. Long QT and short QT syndrome. In: Zipes DP Jalife J eds. Cardiac Electrophysiology: From Cell to Bedside. 5th ed. Philadelphia Pa: Elsevier/Saunders; 2009: 731–744.

2. Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

3. How Really Rare Are Rare Diseases?:

4. KCNH2 -K897T Is a Genetic Modifier of Latent Congenital Long-QT Syndrome

Cited by 238 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. From genes to clinical management: A comprehensive review of long QT syndrome pathogenesis and treatment;Heart Rhythm O2;2024-08

2. PTPRD gene variant rs10739150: A potential game-changer in hypertension diagnosis;PLOS ONE;2024-06-27

3. Bayliss Starling Prize Lecture 2023: Neuropeptide‐Y being ‘unsympathetic’ to the broken hearted;The Journal of Physiology;2024-06-07

4. The Physiological Function of nNOS-Associated CAPON Proteins and the Roles of CAPON in Diseases;International Journal of Molecular Sciences;2023-10-31

5. The role of the neural NO synthase adapter protein in the pathogenesis of metabolic syndrome and type 2 diabetes mellitus;Сибирский научный медицинский журнал;2023-10-27