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Published in 2019 at "Human molecular genetics"
DOI: 10.1093/hmg/ddz125
Abstract: Duchenne muscular dystrophy (DMD) is a rare genetic disease affecting 1 in 3500-5000 newborn boys. It is due to mutations in the DMD gene with a consequent lack of dystrophin protein that leads to deterioration…
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Keywords:
dmd;
dystrophin myostatin;
muscle;
mdx mice ... See more keywords