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M1933 A Comprehensive Analysis of the Phenotypic Manifestations of Mismatch Repair Gene Mutations: Comparing MSH6 with MLH1 and MSH2 Mutation Carriers

✍ Scribed by Kastrinos, Fay; Steyerberg, Ewout W; Balmaña, Judith; Syngal, Sapna

Book ID
123036591
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
73 KB
Volume
136
Category
Article
ISSN
0016-5085

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Mutation analysis of the MLH1, MSH2 and
Mutation analysis of the MLH1, MSH2 and MSH6 genes in patients with double primary cancers of the colorectum and the endometrium: A population-based study in northern Sweden
✍ Kristina Cederquist; Monica Emanuelsson; Ingela Göransson; Elke Holinski-Feder; 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 French ⚖ 105 KB 👁 2 views

## Abstract Hereditary nonpolyposis colorectal cancer (HNPCC) is an autosomal dominant disorder that predisposes to predominantly colorectal and endometrial cancers due to germline mutations in DNA mismatch repair genes, mainly __MLH1__, __MSH2__ and in families with excess endometrial cancer also

Erratum to Cederquist et al., “Mutation
Erratum to Cederquist et al., “Mutation analysis of the MLH1, MSH2 and MSH6 genes in patients with double primary cancers of the colorectum and the endometrium—A population-based study in northern Sweden.” Int J Cancer 2004; 109(3):370–376
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## Abstract The original article to which this Erratum refers was published in International Journal of Cancer (2004) 109(3) 370–376DOI: 10.1002/ijc.11718