載入...
Disease-causing mutations in cardiac troponin T: identification of a critical tropomyosin-binding region.
Fifteen percent of the mutations causing familial hypertrophic cardiomyopathy are in the troponin T gene. Most mutations are clustered between residues 79 and 179, a region known to bind to tropomyosin at the C-terminus near the complex between the N- and C-termini. Nine mutations were introduced in...
Na minha lista:
| Main Authors: | , , , |
|---|---|
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
2001
|
| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1301748/ https://ncbi.nlm.nih.gov/pubmed/11606294 |
| 標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|