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Antisense mediated exon skipping therapy for duchenne muscular dystrophy (DMD)
Camilla Brolin, Takehiko Shiraishi
Transcription, RNA, and Gene Medicine Program
8
Citations (Scopus)
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Medicine & Life Sciences
Animal Models
12%
Antisense Oligonucleotides
41%
Duchenne Muscular Dystrophy
84%
Dystrophin
67%
Exons
60%
Genes
7%
In Vitro Techniques
7%
Morpholinos
23%
Muscle Proteins
21%
Mutation
10%
Peptide Nucleic Acids
26%
Therapeutics
11%
Chemical Compounds
Antisense Oligonucleotide
100%
Lethal
42%
Mutation
30%
Oligomer
28%
Peptide Nucleic Acid
45%
Protein
14%