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Targeted sequencing of genes associated with the mismatch repair pathway in patients with endometrial cancer
Germline variants inactivating the mismatch repair (MMR) genes MLH1, MSH2, MSH6 and PMS2 cause Lynch syndrome that implies an increased cancer risk, where colon and endometrial cancer are the most frequent. Identification of these pathogenic variants is important to identify endometrial cancer patie...
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| Gepubliceerd in: | PLoS One |
|---|---|
| Hoofdauteurs: | , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Public Library of Science
2020
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7340288/ https://ncbi.nlm.nih.gov/pubmed/32634176 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0235613 |
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