Investigation of APC, MLH1 and MSH2 Mutations in Patients with Hereditary Colorectal Carcinoma: A Single Center Experience
Aim:Colorectal cancer (CRC) is the third most common cancer in the world. About 5-6% of all CRCs have a hereditary inheritance related with germline mutations. Mutation screening is carried out with gene panels for CRCs to manage family against to CRCs more effectively. In this study, mutation scree...
Αποθηκεύτηκε σε:
| Κύριος συγγραφέας: | |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Haseki Training and Research Hospital
2021-01-01
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| Σειρά: | Haseki Tıp Bülteni |
| Θέματα: | |
| Διαθέσιμο Online: |
http://www.hasekidergisi.com/archives/archive-detail/article-preview/nvestigation-of-apc-mlh1-and-msh2-mutations-in-pat/43952
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