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A Mononucleotide Markers Panel to Identify hMLH1/hMSH2 Germline Mutations
Hereditary NonPolyposis Colorectal Cancer (Lynch syndrome) is an autosomal dominant disease caused by germline mutations in a class of genes deputed to maintain genomic integrity during cell replication, mutations result in a generalized genomic instability, particularly evident at microsatellite lo...
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| Main Authors: | , , , , , , , , , , , , , , |
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| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
IOS Press
2007
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3850839/ https://ncbi.nlm.nih.gov/pubmed/17473388 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2007/703129 |
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