Author:
MORITA H.,DEPALMA S.R.,ARAD M.,MCDONOUGH B.,BARR S.,DUFFY C.,MARON B.J.,SEIDMAN C.E.,SEIDMAN J.G.
Publisher
Cold Spring Harbor Laboratory
Subject
Genetics,Molecular Biology,Biochemistry
Reference24 articles.
1. Mutations of the Light Meromyosin Domain of the β-Myosin Heavy Chain Rod in Hypertrophic Cardiomyopathy
2. Dracopoli N., Haines J.L., Korf B.R., Moir D.T., Morton C.C., Seidman C.E., Seidman J.G., and Smith D.R., Eds.2002. Searching candidate genes for mutations. Current Protocols in human genetics, Chap. 7. Current Protocols. Wiley and Sons, New York.
3. Fatkin D., Seidman J.G., and Seidman C.E.2000. Hypertrophic cardiomyopathy. In Cardiovascular medicine, 2nd edition (ed. J.T. Willerson and J.N. Cohn), p. 1055. Churchill Livingstone, New York.
4. A molecular basis for familial hypertrophic cardiomyopathy: A β cardiac myosin heavy chain gene missense mutation
5. Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy
Cited by
10 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献