2Schwartz ML, Colan SD. Familial restrictive cardiomyopathy with skeletal abnormalities. Am J Cardiol, 2003, 92: 636-639.
3Daneshvar DA, Kedia G, Fishbein MC, et al. Familial restrictive cardiomyopathy with 12 affected family members. Am J Cardiol, 2012, 109: 445-447.
4Mogensen J, Kubo T, Duque M, et al. Idiopathic restrictive cardiomyopathy is part of the clinical expression of cardiac troponin I mutations. J Clin Invest, 2003, 111:209-216.
5Karam S, Raboisson M J, Ducreux C, et al. A de novo mutation of the beta cardiac myosin heavy chain gene in an infantile restrictive cardiomyopathy. Congenit Heart, 2008, 3:138-143.
6Peddy SB, Vricella LA, Crosson JE, et al. Infantile restrictive cardiomyopathy resulting from a mutation in the cardiac troponin T gene. Pediatrics, 2006, 117:1830-1833.
7Arbustini E, Pasotti M, Pilotto A, et al. Desmin accumulation restrictive cardiomyopathy and atrioventricular block associated with desmin gene defects. Eur J Heart Fail, 2006, 8:477-483.
8Rivenes SM, Kearney DL, Smith EO, et al. Sudden death and cardiovascular collapse in children with restrictive cardiomyopathy. Circulation, 2000, 102: 876-8$2.
9Kaski JP, Syrris P, Burch M, et al. Idiopathic restrictive cardiomyopathy in children is caused by mutations in cardiac sarcomere protein genes. Heart, 2008, 94: 1478-1484.
10Kubo T, Gimeno JR, Bahl A, et al. Prevalence, clinical significance, and genetic basis of hypertrophic cardionyopathy with restrictive phenotype. J Am Coil Cardiol, 2007,49: 2419-2426.
