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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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Dades bibliogràfiques
Autors principals: Clark, Nicole, Wu, Xiling, Her, Chengtao
Format: Artigo
Idioma:Inglês
Publicat: Bentham Science Publishers 2013
Matèries:
Accés en línia: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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