Commonality amid diversity: multi-study proteomic identification of conserved disease mechanisms in spinal muscular atrophy
(2016)
Journal Article
Fuller, H., Wishart, T., & Gillingwater, T. (2016). Commonality amid diversity: multi-study proteomic identification of conserved disease mechanisms in spinal muscular atrophy. Neuromuscular Disorders, 560-569. https://doi.org/10.1016/j.nmd.2016.06.004
The neuromuscular disease spinal muscular atrophy (SMA) is a leading genetic cause of infant mortality, resulting from low levels of full-length survival motor neuron (SMN) protein. Despite having a good understanding of the underlying genetics of SM... Read More about Commonality amid diversity: multi-study proteomic identification of conserved disease mechanisms in spinal muscular atrophy.