Citations for
1VCL, CMD1W
Identification of a metavinculin missense mutation, R975W, associated with both hypertrophic and dilated cardiomyopathy.
Vasile VC, Will ML, Ommen SR, Edwards WD, Olson TM, Ackerman MJ.
Mol Genet Metab 87(2):169-74. Epub 2005 Oct 19. 2006
2VCLM, CMD1W
Obstructive hypertrophic cardiomyopathy is associated with reduced expression of vinculin in the intercalated disc.
Vasile VC, Edwards WD, Ommen SR, Ackerman MJ.
Biochem Biophys Res Commun 349(2):709-15. Epub 2006 Aug 24. 2006
3MYH6, PLN, CMH6, CMD1W
Molecular genetics and genomics of heart failure.
Liew CC, Dzau VJ.
Nat Rev Genet 5(11):811-25. 2004
4CMD1W, CMH1, CMH2, VCL
Dilated cardiomyopathy: a genetically heterogeneous disease.
Shaw T,Elliott P,McKenna WJ.
Lancet 360(31):654-655. 2002