Citations for
1ACTA2, MYMY5
Analysis of ACTA2 in European Moyamoya disease patients.
Roder C, Peters V, Kasuya H, Nishizawa T, Wakita S, Berg D, Schulte C, Khan N, Tatagiba M, Krischek B.
Eur J Paediatr Neurol 15(2):117-22. doi: 10.1016/j.ejpn.2010.09.002. Epub 2010 Oct 20. 2011
2MYMY1, MYMY2, MYMY3, MYMY5, MYMY6
Genetics of Moyamoya disease.
Roder C, Nayak NR, Khan N, Tatagiba M, Inoue I, Krischek B.
J Hum Genet 55(11):711-6. Epub 2010 Aug 26. 2010
3ACTA2, MSMD1, MYMY5, TAAD4
Mutations in smooth muscle alpha-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic disease.
Guo DC, Papke CL, Tran-Fadulu V, Regalado ES, Avidan N, Johnson RJ, Kim DH, Pannu H, Willing MC, Sparks E, Pyeritz RE, Singh MN, Dalman RL, Grotta JC, Marian AJ, Boerwinkle EA, Frazier LQ, LeMaire SA, Coselli JS, Estrera AL, Safi HJ, Veeraraghavan S, Muzny DM, Wheeler DA, Willerson JT, Yu RK, Shete SS, Scherer SE, Raman CS, Buja LM, Milewicz DM.
Am J Hum Genet 84(5):617-27. doi: 10.1016/j.ajhg.2009.04.007. Epub 2009 Apr 30. 2009