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Mixed methods formative evaluation of a collaborative care program to decrease risky opioid prescribing and increase non-pharmacologic approaches to pain management.
Repeated TALEs: visualizing DNA sequence localization and chromosome dynamics in live cells.
Whole-genome sequencing identifies a novel ABCB7 gene mutation for X-linked congenital cerebellar ataxia in a large family of Mongolian ancestry.
Phase 1 study of the safety, tolerability, and pharmacokinetics of TH-302, a hypoxia-activated prodrug, in patients with advanced solid malignancies.
Precision of Exon Skipping with U7 Constructs.
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Precision of Exon Skipping with U7 Constructs.
Flotte TR. Precision of Exon Skipping with U7 Constructs. Hum Gene Ther. 2021 11; 32(21-22):1315-1316.
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PubMed
subject areas
Dystrophin
Exons
Humans
Muscular Dystrophy, Duchenne
authors with profiles
Terence R Flotte MD