dc.date.accessioned2020-03-11T20:37:42Z
dc.date.accessioned2022-10-18T23:06:37Z
dc.date.available2020-03-11T20:37:42Z
dc.date.available2022-10-18T23:06:37Z
dc.date.created2020-03-11T20:37:42Z
dc.date.issued2008
dc.identifierhttp://hdl.handle.net/10533/241377
dc.identifier15010006
dc.identifierWOS:000257180900008
dc.identifierno scielo
dc.identifiereid=2-s2.0-49249136904
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4472716
dc.description.abstractGermline 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.languageeng
dc.relationhttps://doi.org/10.4161/epi.3.3.6387
dc.relation10.4161/epi.3.3.6387
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 Chile
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.titlePromoter hypermethylation of BRCA1 correlates with absence of expression in hereditary breast cancer tumors.
dc.typeArticulo


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