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Chapter 15 Brain Tumors and the Lynch Syndrome

dc.contributor.authorPeltomäki, Päivi
dc.contributor.authorGylling, Annette
dc.date.accessioned2025-03-08T07:29:45Z
dc.date.available2025-03-08T07:29:45Z
dc.date.issued2011
dc.date.submitted2019-10-04 14:27:25
dc.date.submitted2020-04-01T14:07:02Z
dc.date.submitted2016-08-01 23:55
dc.date.submitted2019-10-04 14:27:25
dc.date.submitted2020-04-01T14:07:02Z
dc.date.submitted2016-12-31 23:55:55
dc.date.submitted2019-10-04 14:27:25
dc.date.submitted2020-04-01T14:07:02Z
dc.identifier612584
dc.identifierOCN: 1030821093
dc.identifierhttp://library.oapen.org/handle/20.500.12657/32348
dc.identifier.urihttps://doab-dev.siscern.org/handle/20.500.12854/187303
dc.description.abstractLynch syndrome (LS) (MIM No. 120435-6), previously known as hereditary nonpolyposis colorectal cancer (HNPCC) (Boland, 2005), is an autosomal dominant disorder caused by germline mutation in one of the DNA mismatch repair (MMR) genes. LS is among the most prevalent cancer syndromes in man and is estimated to account for 1-6% of all colorectal cancers (Lynch & de la Chapelle, 2003).
dc.languageEnglish
dc.rightsopen access
dc.subject.otherbrain tumors
dc.subject.otherlynch syndrome
dc.subject.otherbrain tumors
dc.subject.otherlynch syndrome
dc.subject.otherColorectal cancer
dc.subject.otherDNA methylation
dc.subject.otherDNA mismatch repair
dc.subject.otherGene
dc.subject.otherGlioblastoma
dc.subject.otherGlioma
dc.subject.otherHereditary nonpolyposis colorectal cancer
dc.subject.otherMutation
dc.subject.otherNeoplasm
dc.subject.otherthema EDItEUR::P Mathematics and Science::PD Science: general issues
dc.titleChapter 15 Brain Tumors and the Lynch Syndrome
dc.typechapter
oapen.identifier.doi10.5772/21293
oapen.relation.isPublishedBy035ecc65-6737-43cf-a13a-6bdf67ce01f4
oapen.relation.isPartOfBook3afefdf6-fff0-4e5b-9a2e-bbc9a5675dc3
oapen.relation.isFundedByfb214456-da48-4ff7-a1ee-f6407a27f6be
oapen.relation.isFundedBy7292b17b-f01a-4016-94d3-d7fb5ef9fb79
oapen.collectionEuropean Research Council (ERC)
oapen.grant.number232635
oapen.grant.programFP7
dc.relationisFundedBy7292b17b-f01a-4016-94d3-d7fb5ef9fb79
dc.chapternumber1


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