تحميل...
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...
محفوظ في:
| المؤلفون الرئيسيون: | , , , , , , |
|---|---|
| التنسيق: | Artigo |
| اللغة: | Inglês |
| منشور في: |
BMJ Group
2006
|
| الموضوعات: | |
| الوصول للمادة أونلاين: | 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 |
| الوسوم: |
إضافة وسم
لا توجد وسوم, كن أول من يضع وسما على هذه التسجيلة!
|