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Published in 2022 at "Human gene therapy"
DOI: 10.1089/hum.2022.069
Abstract: Myotonic dystrophy type 1 (DM1) is a neuromuscular disorder that affects many organs. It is caused by the expansion of a cytosine-thymine-guanine (CTG) triplet repeat in the 3' untranslated region (UTR) of the human myotonic…
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Keywords:
dystrophy type;
mutant hdmpk;
ionis 877864;
myotonic dystrophy ... See more keywords