Author:
Murphy Ross T.,Mogensen Jens,McGarry Kate,Bahl Ajay,Evans Alison,Osman Eyman,Syrris Petros,Gorman Grainne,Farrell Michael,Holton Janice L.,Hanna Michael G.,Hughes Sian,Elliott Perry M.,MacRae Calum A.,McKenna William J.
Subject
Cardiology and Cardiovascular Medicine
Reference21 articles.
1. Novel PRKAG2 mutation responsible for the genetic syndrome of ventricular preexcitation and conduction system disease with childhood onset and absence of cardiac hypertrophy;Gollob;Circulation,2001
2. Constitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathy;Arad;J Clin Invest,2002
3. Identification of a gene responsible for familial Wolff-Parkinson-White syndrome;Gollob;N Engl J Med,2001
4. Transgenic mice overexpressing mutant PRKAG2 define the cause of Wolff-Parkinson-White syndrome in glycogen storage cardiomyopathy;Arad;Circulation,2003
5. Vosberg HP, McKenna WJ. Cardiomyopathies. In: Rimon DL, Connor JM, Pyeritz RE, Korf BR, editors. Emery and Rimoin's Principles and Practice of Medical Genetics. 4th edition. London: Churchill Livingstone, 2002:1342–416.
Cited by
138 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