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Germline mismatch repair gene variants analyzed by universal sequencing in Japanese cancer patients
BACKGROUND: Lynch syndrome (LS) is the commonest inherited cancer syndrome caused by pathogenic variants of germline DNA mismatch repair (g.MMR) genes. Genome‐wide sequencing is now increasingly applied for tumor characterization, but not for g.MMR. The aim of this study was to evaluate the incidenc...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Cancer Med |
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| Κύριοι συγγραφείς: | , , , , , , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
John Wiley and Sons Inc.
2019
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6745857/ https://ncbi.nlm.nih.gov/pubmed/31386297 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/cam4.2432 |
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