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...
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| Hlavní autor: | |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Haseki Training and Research Hospital
2021-01-01
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| Edice: | Haseki Tıp Bülteni |
| Témata: | |
| On-line přístup: |
http://www.hasekidergisi.com/archives/archive-detail/article-preview/nvestigation-of-apc-mlh1-and-msh2-mutations-in-pat/43952
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