Citations for
1CMH10, MYL2
Cardiomyopathy-linked myosin regulatory light chain mutations disrupt myosin strain-dependent biochemistry.
Greenberg MJ, Kazmierczak K, Szczesna-Cordary D, Moore JR.
Proc Natl Acad Sci U S A 107(40):17403-8. Epub 2010 Sep 20. 2010
2CMH10, MYL2
Familial hypertrophic cardiomyopathy-linked alterations in Ca2+ binding of human cardiac myosin regulatory light chain affect cardiac muscle contraction.
Szczesna-Cordary D, Guzman G, Ng SS, Zhao J.
J Biol Chem 279(5):3535-42. Epub 2003 Nov 1. 2004
3CMH8, CMH10, MYL2, MYL3
Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle.
Poetter K, et al.
Nat Genet 13 : 63-68. 1996