Suspected Lynch syndrome associated MSH6 variants: A functional assay to determine their pathogenicity-Reference-Cited by-同舟云学术

Suspected Lynch syndrome associated MSH6 variants: A functional assay to determine their pathogenicity

Published:2017-05-22 Issue:5 Volume:13 Page:e1006765
ISSN:1553-7404
Container-title:PLOS Genetics
language:en
Short-container-title:PLoS Genet

Author:

Houlleberghs Hellen,Goverde Anne^ORCID,Lusseveld Jarnick,Dekker Marleen^ORCID,Bruno Marco J.,Menko Fred H.,Mensenkamp Arjen R.^ORCID,Spaander Manon C. W.,Wagner Anja,Hofstra Robert M. W.,te Riele Hein^ORCID

Funder

KWF Kankerbestrijding

Publisher

Public Library of Science (PLoS)

Subject

Cancer Research,Genetics (clinical),Genetics,Molecular Biology,Ecology, Evolution, Behavior and Systematics

Reference53 articles.

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3. The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer;R Fishel;Cell,1993

4. Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer;M Miyaki;Nat Genet,1997

5. EPCAM germline and somatic rearrangements in Lynch syndrome : identification of a novel 3'EPCAM deletion;M Spaepen;Genes Chromosom Cancer,2013

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