A DYNC1H1 mutation in autosomal dominant spinal muscular atrophy shows the potential of pharmacological inhibition of histone deacetylase 6 as a treatment for disease associated cellular phenotypes
Green, R., Simoes, F. A., Reyes-Aldasoro, C. C. , Rossor, A. M., Scoto, M., Barri, M., Greensmith, L., Muntoni, F., Reilly, M. M. & Hafezparast, M. (2016). A DYNC1H1 mutation in autosomal dominant spinal muscular atrophy shows the potential of pharmacological inhibition of histone deacetylase 6 as a treatment for disease associated cellular phenotypes. Journal Of The Peripheral Nervous System, 21(3), pp. 229-314. doi: 10.1111/jns.12181
| Publication Type: | Article |
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| Additional Information: | This is the peer reviewed version of the following article: Green, R., Simoes, F. A., Reyes-Aldasoro, C. C., Rossor, A. M., Scoto, M., Barri, M., Greensmith, L., Muntoni, F., Reilly, M. M. & Hafezparast, M. (2016). A DYNC1H1 mutation in autosomal dominant spinal muscular atrophy shows the potential of pharmacological inhibition of histone deacetylase 6 as a treatment for disease associated cellular phenotypes. Journal Of The Peripheral Nervous System, 21(3), pp. 261-262., which is published in final form at http://dx.doi.org/10.1111/jns.12181. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving. |
| Subjects: | R Medicine > RC Internal medicine T Technology > TK Electrical engineering. Electronics Nuclear engineering |
| Departments: | School of Science & Technology > Engineering School of Science & Technology > Computer Science > giCentre |
| SWORD Depositor: |
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