ロード中...
Effects of Pathogenic Proline Mutations on Myosin Assembly
Laing distal myopathy (MPD1) is a genetically dominant myopathy characterized by early and selective weakness of the distal muscles. Mutations in the MYH7 gene encoding for the β-myosin heavy chain are the underlying genetic cause of MPD1. However, their pathogenic mechanisms are currently unknown....
保存先:
| 主要な著者: | , , |
|---|---|
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2011
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3267876/ https://ncbi.nlm.nih.gov/pubmed/22155079 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jmb.2011.11.042 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|