Human γ2-AMPK Mutations
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Publisher
Springer New York
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http://link.springer.com/content/pdf/10.1007/978-1-4939-7598-3_37
Reference91 articles.
1. Elliott PM, Anastasakis A, Borger MA, Borggrefe M, Cecchi F, Charron P, Hagege AA, Lafont A, Limongelli G, Mahrholdt H, McKenna WJ, Mogensen J, Nihoyannopoulos P, Nistri S, Pieper PG, Pieske B, Rapezzi C, Rutten FH, Tillmanns C, Watkins H (2014) 2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy: the Task Force for the Diagnosis and Management of Hypertrophic Cardiomyopathy of the European Society of Cardiology (ESC). Eur Heart J 35(39):2733–2779. https://doi.org/10.1093/eurheartj/ehu284
2. Watkins H, Ashrafian H, Redwood C (2011) Inherited cardiomyopathies. N Engl J Med 364(17):1643–1656. https://doi.org/10.1056/NEJMra0902923
3. Maron BJ (2015) Historical perspectives on sudden deaths in young athletes with evolution over 35 years. Am J Cardiol 116(9):1461–1468. https://doi.org/10.1016/j.amjcard.2015.07.072
4. Thierfelder L, Watkins H, MacRae C, Lamas R, McKenna W, Vosberg HP, Seidman JG, Seidman CE (1994) Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere. Cell 77(5):701–712
5. Ashrafian H, Watkins H (2007) Reviews of translational medicine and genomics in cardiovascular disease: new disease taxonomy and therapeutic implications cardiomyopathies: therapeutics based on molecular phenotype. J Am Coll Cardiol 49(12):1251–1264. https://doi.org/10.1016/j.jacc.2006.10.073 . S0735-1097(07)00130-1 [pii]
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