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A comparison of CDKN2A mutation detection within the Melanoma Genetics Consortium (GenoMEL)
CDKN2A is the major melanoma susceptibility gene so far identified, but only 40% of three or more case families have identified mutations. A comparison of mutation detection rates was carried out by “blind” exchange of samples across GenoMEL, the Melanoma Genetics Consortium, to establish the false...
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| Huvudupphovsmän: | , , , , , , , , , , , , , , , , , , , , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
2008
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2494985/ https://ncbi.nlm.nih.gov/pubmed/18394881 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ejca.2008.03.005 |
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