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MutS Homologues hMSH4 and hMSH5: Genetic Variations, Functions, and Implications in Human Diseases
The prominence of the human mismatch repair (MMR) pathway is clearly reflected by the causal link between MMR gene mutations and the occurrence of Lynch syndrome (or HNPCC). The MMR family of proteins also carries out a plethora of diverse cellular functions beyond its primary role in MMR and homolo...
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| Hauptverfasser: | , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Bentham Science Publishers
2013
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3637681/ https://ncbi.nlm.nih.gov/pubmed/24082819 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2174/1389202911314020002 |
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