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Complex splicing pattern generates great diversity in human NF1 transcripts
BACKGROUND: Mutation analysis of the neurofibromatosis type 1 (NF1) gene has shown that about 30% of NF1 patients carry a splice mutation resulting in the production of one or several shortened transcripts. Some of these transcripts were also found in fresh lymphocytes of healthy individuals, albeit...
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| Hlavní autoři: | , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2002
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC115845/ https://ncbi.nlm.nih.gov/pubmed/12057013 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-3-13 |
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