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December 23, 2016

FDA OKs first treatment for rare genetic disorder

AP Health News - Fetched: December 23rd, 2016, 8:00pm UTC
WASHINGTON (AP) -- The Food and Drug Administration on Friday approved the first treatment for children and adults with spinal muscular atrophy, a rare genetic disorder marked by progressive muscle weakness thatamp;apos;s the most common genetic cause of death in infants....

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