Genetic association analyses highlight biological pathways underlying mitral valve prolapse
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://www.nature.com/articles/ng.3383.pdf
Reference38 articles.
1. Freed, L.A. et al. Mitral valve prolapse in the general population: the benign nature of echocardiographic features in the Framingham Heart Study. J. Am. Coll. Cardiol. 40, 1298–1304 (2002).
2. Disse, S. et al. Mapping of a first locus for autosomal dominant myxomatous mitral valve prolapse to chromosome 16p11.2-p12.1. Am. J. Hum. Genet. 65, 1242–1251 (1999).
3. Freed, L.A. et al. A locus for autosomal dominant mitral valve prolapse on chromosome 11p15.4. Am. J. Hum. Genet. 72, 1551–1559 (2003).
4. Kyndt, F. et al. Mapping of X-linked myxomatous valvular dystrophy to chromosome Xq28. Am. J. Hum. Genet. 62, 627–632 (1998).
5. Nesta, F. et al. New locus for autosomal dominant mitral valve prolapse on chromosome 13: clinical insights from genetic studies. Circulation 112, 2022–2030 (2005).
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