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Whole-exome sequencing identified a novel mutation of MLH1 in an extended family with lynch syndrome
Hereditary nonpolyposis colorectal cancer or Lynch syndrome is autosomal dominant cancer predisposition syndrome characterized by early onset of colorectal cancer and neoplasia in other organs. This condition typically caused by germline mutations in the mismatch repair genes MLH1, MSH2, MSH6, and P...
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| Publicat a: | Genes Dis |
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| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Chongqing Medical University
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7729095/ https://ncbi.nlm.nih.gov/pubmed/33335961 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.gendis.2019.07.011 |
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