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Green, R, Simoes, F, Reyes-Aldosoro, C, Rossor, A, Barri, M, Sedlakova, Z, Greensmith, L, Muntoni, F, Reilly, M and 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. In: 27th International Symposium on ALS/MND, 7-9 Dec 2016, Dublin.