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Dokumenttyp:
Journal Article
Autor(en):
Morak, Monika; Käsbauer, Sarah; Kerscher, Martina; Laner, Andreas; Nissen, Anke M; Benet-Pagès, Anna; Schackert, Hans K; Keller, Gisela; Massdorf, Trisari; Holinski-Feder, Elke
Titel:
Loss of MSH2 and MSH6 due to heterozygous germline defects in MSH3 and MSH6.
Abstract:
Lynch Syndrome (LS) is the most common dominantly inherited colorectal cancer (CRC) predisposition and is caused by a heterozygous germline defect in one of the DNA mismatch repair (MMR) genes MLH1, MSH2, MSH6, or PMS2. High microsatellite instability (MSI-H) and loss of MMR protein expression in tumours reflecting a defective MMR are indicators for LS, as well as a positive family history of early onset CRC. MSH2 and MSH6 form a major functional heterodimer, and MSH3 is an alternative binding p...     »
Zeitschriftentitel:
Fam Cancer
Jahr:
2017
Band / Volume:
16
Heft / Issue:
4
Seitenangaben Beitrag:
491-500
Sprache:
eng
Volltext / DOI:
doi:10.1007/s10689-017-9975-z
PubMed:
http://view.ncbi.nlm.nih.gov/pubmed/28528517
Print-ISSN:
1389-9600
TUM Einrichtung:
Institut für Allgemeine Pathologie und Pathologische Anatomie
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