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Lynch Syndrome-Related Clear Cell Carcinoma of the Cervix: A Case Report
Lynch syndrome, a hereditary cancer syndrome, occurs because of germline mutations in at least one of four DNA mismatch repair genes (MutL Homolog 1 (MLH1), MutS Homolog 2 (MSH2), MutS Homolog 6 (MSH6), and PMS1 Homolog 2 (PMS2)). The disorder is associated with colorectal, endometrial, and other ep...
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| Publicat a: | Int J Mol Sci |
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| Autors principals: | , , , , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
MDPI
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5979360/ https://ncbi.nlm.nih.gov/pubmed/29587389 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms19040979 |
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