Wordt geladen...
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....
Bewaard in:
| Hoofdauteurs: | , , |
|---|---|
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2011
|
| Onderwerpen: | |
| Online toegang: | 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 |
| Tags: |
Voeg label toe
Geen labels, Wees de eerste die dit record labelt!
|