Journal
NEUROLOGY
Volume 94, Issue 12, Pages 538-540Publisher
LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1212/WNL.0000000000009139
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Duchenne muscular dystrophy (DMD) is a degenerative muscle disease with over 65% of patients having a deletion of one or more exons within the DMD gene.(1) Exon deletions that disrupt the reading frame cause rapid mRNA degradation with no functional dystrophin protein produced.
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