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Founder Mutations in Xeroderma Pigmentosum
In this issue, Soufir et al. report a founder mutation in the XPC DNA repair gene in 74% of families with xeroderma pigmentosum (XP) in the Maghreb region (Algeria, Morocco, and Tunisia) of northern Africa. These patients have a high frequency of skin cancer. The presence of this founder mutation pr...
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| Hlavní autoři: | , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2010
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3486739/ https://ncbi.nlm.nih.gov/pubmed/20463673 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/jid.2010.76 |
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