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Published in 2019 at "Pediatric Pulmonology"
DOI: 10.1002/ppul.24203
Abstract: Spinal Muscular Atrophy type 1 (SMA1) is a rare genetic neuromuscular disease where 75% of SMA1 patients die/require permanent‐ventilation by 13.6 months. This study assessed the health outcomes of SMA1 infants treated with AVXS‐101 gene…
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Keywords:
health outcomes;
spinal muscular;
avxs 101;
atrophy type ... See more keywords