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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....
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| Main Authors: | , , |
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| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
2011
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| 主題: | |
| 在線閱讀: | 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 |
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