CANCER MAMMAIRE ET LA MUTATION BRCA1

dc.contributor.authorBENATTIA, IMANE
dc.contributor.authorBOUAZZA, NOUR EL HOUDA
dc.date.accessioned2019-01-06T12:58:01Z
dc.date.available2019-01-06T12:58:01Z
dc.date.issued2017
dc.description.abstractIn Algeria, breast cancer is the most frequent malignant tumor and the leading cause of cancer death in women. It is a complex and heterogeneous disease. This heterogeneity is found at the histological, phenotypic and molecular level. It remains an ill-known disease and the current clinical and histological classifications do not allow to predict the prognostic and predictive parameters. The predisposition to breast cancer is inherited as a dominant trait.The presence of mutations with founding effect in the founding populations facilitates the discovery of highly penetrating alleles in high-risk individuals within families with a hereditary susceptibility to breast cancer. Our goal is to do a theoretical study on the mammary gland, demonstrated the importance of breast cancer and its relationship with the mutation BRCA1en_US
dc.identifier.urihttp://e-biblio.univ-mosta.dz/handle/123456789/8082
dc.language.isofren_US
dc.subjectBreast Glanden_US
dc.subjectBreast Canceren_US
dc.subjectMutation BRCA1en_US
dc.subjectGlande Mammaireen_US
dc.subjectCancer Mammaireen_US
dc.subjectMutation BRCA1en_US
dc.titleCANCER MAMMAIRE ET LA MUTATION BRCA1en_US
dc.typeOtheren_US

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