Identification of Splicing Factors Involved in DMD Exon Skipping Events Using an In Vitro RNA Binding Assay
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Publisher
Springer New York
Link
http://link.springer.com/content/pdf/10.1007/978-1-4939-7374-3_11
Reference12 articles.
1. Flanigan KM, Dunn DM, von Niederhausern A et al (2011) Nonsense mutation-associated Becker muscular dystrophy: interplay between exon definition and splicing regulatory elements within the DMD gene. Hum Mutat 32:299–308. doi: 10.1002/humu.21426
2. Disset A, Bourgeois CF, Benmalek N et al (2006) An exon skipping-associated nonsense mutation in the dystrophin gene uncovers a complex interplay between multiple antagonistic splicing elements. Hum Mol Genet 15:999–1013. doi: 10.1093/hmg/ddl015
3. Miro J, Laaref AM, Rofidal V et al (2015) FUBP1: a new protagonist in splicing regulation of the DMD gene. Nucleic Acids Res 43:2378–2389. doi: 10.1093/nar/gkv086
4. Guiraud S, Chen H, Burns DT, Davies KE (2015) Advances in genetic therapeutic strategies for Duchenne muscular dystrophy. Exp Physiol 100:1458–1467. doi: 10.1113/EP085308
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2. The position of nonsense mutations can predict the phenotype severity: A survey on the DMD gene;PLOS ONE;2020-08-19
3. Application whole exome sequencing for the clinical molecular diagnosis of patients with Duchenne muscular dystrophy; identification of four novel nonsense mutations in four unrelated Chinese DMD patients;Molecular Genetics & Genomic Medicine;2019-04
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