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DCTN1-related neurodegeneration: Perry syndrome and beyond
Perry syndrome (PS) is a rare hereditary neurodegenerative disease characterized by autosomal dominant parkinsonism, psychiatric symptoms, weight loss, central hypoventilation, and distinct TDP-43 pathology. The mutated causative gene for PS is DCTN1, which encodes the dynactin subunit p150(Glued)....
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| Foilsithe in: | Parkinsonism Relat Disord |
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| Main Authors: | , , , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
2017
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5546300/ https://ncbi.nlm.nih.gov/pubmed/28625595 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.parkreldis.2017.06.004 |
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