New advances in medication for muscle disease in children Spinraza, the gene therapy medication, also provides significant improvements in cases with the next most severe form of neuromuscular disease, spinal muscular atrophy (SMA), which afflicts children from 6 to 18 months of age. http://ift.tt/eA8V8J
Monday 26 February 2018
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# Latest Science News -- ScienceDaily
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