טוען...
Consequences of the DYT1 mutation on torsinA oligomerization and degradation
DYT1 is the most common inherited dystonia, a neurological syndrome that causes disabling involuntary muscle contractions. This autosomal dominant disease is caused by a glutamic acid deletion near the carboxy-terminus in the protein torsinA. Cell and animal based studies have shown how the DYT1 mut...
שמור ב:
| Main Authors: | , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
2008
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2605671/ https://ncbi.nlm.nih.gov/pubmed/18940237 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neuroscience.2008.09.028 |
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