Characterization of Familial Hypertrophic Cardiomyopathy on Myosin Essential Light Chain Mutation (A57G)
碩士 === 慈濟大學 === 醫學研究所 === 96 === Familial hypertrophic cardiomyopathy (FHC) is an autosomal dominant disease characterized by left ventricular hypertrophy, myofibrillar disarray, and sudden cardiac death. It is caused by missense mutations in various genes that code for sarcomereic proteins such as...
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| Format: | Others |
| Language: | zh-TW |
| Online Access: | http://ndltd.ncl.edu.tw/handle/45887447354378898006 |