id	author	title	date	pages	extension	mime	words	sentences	flesch	summary	cache	txt
work_faqqesvpdnhvxm63tumovblmim	Baozhong Xin	Homozygosity for a novel splice site mutation in the cardiac myosin-binding protein C gene causes severe neonatal hypertrophic cardiomyopathy	2007	6	.pdf	application/pdf	4345	379	56	Cardiac Myosin-Binding Protein C Gene Causes Severe homozygous splice site mutation in the MYBPC3 gene. block contained MYBPC3, a previously identified cardiomyopathy related gene. for a novel splice site mutation in the cardiac myosin-binding protein C gene causes severe neonatal One of most common genetic causes for hypertrophic cardiomyopathy involves mutations in cardiac myosin-binding protein C (MYBPC3) gene [Charron Homozygous mutation in the MYBPC3 gene causing severe affected individuals at the current time, the consequence of the mutation was determined using 1. Pedigrees of the three families used in the mapping study and mutational analysis of hypertrophic cardiomyopathy. mutation is associated with familial hypertrophic cardiomyopathy. cardiac myosin binding protein C gene (MYBPC3) and hypertrophic cardiomyopathy related to the cardiac myosinbinding protein C gene. cardiac myosin-binding protein C mutation carriers with the myosin binding protein-C gene is responsible for hypertrophic cardiomyopathy with left ventricular dysfunction and Mutations in the cardiac myosin binding protein-C gene on	./cache/work_faqqesvpdnhvxm63tumovblmim.pdf	./txt/work_faqqesvpdnhvxm63tumovblmim.txt