Author:
Yu B,French J A,Carrier L,Jeremy R W,McTaggart D R,Nicholson M R,Hambly B,Semsarian C,Richmond D R,Schwartz K,Trent R J
Subject
Genetics(clinical),Genetics
Reference21 articles.
1. A molecular basis for familial hypertrophic cardiomyopathy: a 1 cardiac myosin heavy chain gene missense mutation;Geisterfer-Lowrance, A.A.T.; Kass, S.; Tanigawa, G.;Cell,1990
2. a-Tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere;ThierfelderL, Watitns H.; C, MacRae;CeU,1994
3. Molecular basis of familial cardiomyopathies;Schwartz, K.; CarrierL, Guicheney; P, Komajda; M.;Circulation,1995
4. Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11;CarrierL, Hengstenberg C.; JS, Beckmann; etal;Nat Genet,1993
5. Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy;Watkins, H.; Conner, D.; ThierfeldeLr, etal;Nat Genet,1995
Cited by
56 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