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Search results
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DMD antisense oligonucleotide mediated exon skipping efficiency correlates with flanking intron retention time and target position within the exon
Integrating whole-genome sequencing in clinical genetics
Integrating Whole-Genome Sequencing in Clinical Genetics: A Novel Disruptive Structural Rearrangement Identified in the Dystrophin Gene (DMD)
Case report: the genetic diagnosis of duchenne muscular dystrophy in the Middle East
Developing tissue specific antisense oligonucleotide-delivery to refine treatment for Duchenne muscular dystrophy
Non-uniform muscle fat replacement along the proximodistal axis in Duchenne muscular dystrophy
Exon skipping: a first in class strategy for Duchenne muscular dystrophy
Adenoviral vectors as genome editing tools : repairing defective DMD alleles
The Pathogenesis and Therapy of Muscular Dystrophies
Muscle MRI in Duchenne and Becker muscular dystrophy
The TREAT-NMD DMD Global Database: Analysis of More than 7,000 Duchenne Muscular Dystrophy Mutations
A 3-base pair deletion, c.9711_9713del, in DMD results in intellectual disability without muscular dystrophy
The TREAT-NMD Duchenne Muscular Dystrophy Registries: Conception, Design, and Utilization by Industry and Academia
Refinement of antisense oligonucleotide mediated exon skipping as therapy for Duchenne muscular dystrophy
Application of microarray-based gene expression technology to neuromuscular disorders
Detecting copy number changes in genomic DNA - MAPH and MLPA
