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Genetic Alterations of δ-Catenin/NPRAP/Neurojungin (CTNND2): Functional Implications in Complex Human Diseases
Some genes involved in complex human diseases are particularly vulnerable to genetic variations such as single nucleotide polymorphism, copy number variations, and mutations. For example, Ras mutations account for over 30% of all human cancers. Additionally, there are some genes that can display dif...
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| Veröffentlicht in: | Hum Genet |
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| Hauptverfasser: | , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2016
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5021578/ https://ncbi.nlm.nih.gov/pubmed/27380241 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-016-1705-3 |
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