Splicing analysis disclosed a determinant single nucleotide for exon skipping caused by a novel intraexonic four‐nucleotide deletion in the dystrophin gene

BACKGROUND: Mutations in exonic splicing enhancer sequences are known to cause splicing errors. Although exonic splicing enhancers have been identified as a stretch of purine‐rich sequences, it has been difficult to precisely pinpoint the determinant nucleotides in these sequences. This article repo...

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Hlavní autoři: Van Khanh Tran, Takeshima, Yasuhiro, Zhang, Zhujun, Yagi, Mariko, Nishiyama, Atsushi, Habara, Yasuaki, Matsuo, Masafumi
Médium: Artigo
Jazyk:Inglês
Vydáno: BMJ Group 2006
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Original Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2563197/
https://ncbi.nlm.nih.gov/pubmed/16738009
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2006.042317
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