Monday, February 26, 2018

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.



from Top Health News – ScienceDaily http://bit.ly/2ERwREB
from Tumblr http://bit.ly/2CorZoX

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