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Functional analysis of splicing mutations in exon 7 of NF1 gene
BACKGROUND: Neurofibromatosis type 1 is one of the most common autosomal dominant disorders, affecting about 1:3,500 individuals. NF1 exon 7 displays weakly defined exon-intron boundaries, and is particularly prone to missplicing. METHODS: In this study we investigated the expression of exon 7 trans...
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| Autori principali: | , , , , , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2007
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1802069/ https://ncbi.nlm.nih.gov/pubmed/17295913 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-8-4 |
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