Related references
Note: Only part of the references are listed.Nonsense Mutation-Associated Becker Muscular Dystrophy: Interplay Between Exon Definition and Splicing Regulatory Elements within the DMD Gene
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Protein, and mRNABased phenotype-genotype correlations in DMD/DMD with point mutations and molecular basis for BMD with nonsense and frameshift mutations in the DMD gene
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Nonclassical splicing mutations in the coding and noncoding regions of the ATM gene: Maximum entropy estimates of splice junction strengths
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Diagnosis of Duchenne dystrophy by enhanced detection of small mutations
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A novel splice site mutation (3157+1G > T) in the dystrophin gene causing total exon skipping and DMD phenotype
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