dc.date.accessioned | 2020-03-11T20:37:42Z | |
dc.date.accessioned | 2022-10-18T23:06:37Z | |
dc.date.available | 2020-03-11T20:37:42Z | |
dc.date.available | 2022-10-18T23:06:37Z | |
dc.date.created | 2020-03-11T20:37:42Z | |
dc.date.issued | 2008 | |
dc.identifier | http://hdl.handle.net/10533/241377 | |
dc.identifier | 15010006 | |
dc.identifier | WOS:000257180900008 | |
dc.identifier | no scielo | |
dc.identifier | eid=2-s2.0-49249136904 | |
dc.identifier.uri | https://repositorioslatinoamericanos.uchile.cl/handle/2250/4472716 | |
dc.description.abstract | Germline mutations in BRCA1 account for a low proportion of hereditary cases in diverse populations. Several efforts have been made to find new genes involved in the inheritance of breast cancer with no success until today. The participation of BRCA1 in t | |
dc.language | eng | |
dc.relation | https://doi.org/10.4161/epi.3.3.6387 | |
dc.relation | 10.4161/epi.3.3.6387 | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.rights | Atribución-NoComercial-SinDerivadas 3.0 Chile | |
dc.rights | http://creativecommons.org/licenses/by-nc-nd/3.0/cl/ | |
dc.title | Promoter hypermethylation of BRCA1 correlates with absence of expression in hereditary breast cancer tumors. | |
dc.type | Articulo | |