Novel biallelic mutations inMSH6 andPMS2 genes: gene conversion as a likely cause ofPMS2 gene inactivation-Reference-Cited by-同舟云学术

Novel biallelic mutations inMSH6 andPMS2 genes: gene conversion as a likely cause ofPMS2 gene inactivation

Published:2007 Issue:11 Volume:28 Page:1084-1090
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Auclair Jessie,Leroux Dominique,Desseigne Françoise,Lasset Christine,Saurin Jean Christophe,Joly Marie Odile,Pinson Stéphane,Xu Xiao Li,Montmain Gilles,Ruano Eric,Navarro Claudine,Puisieux Alain,Wang Qing

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference30 articles.

1. Two PMS2 Mutations in a Turcot Syndrome Family with Small Bowel Cancers

2. Early-Onset Brain Tumor and Lymphoma in MSH2-Deficient Children

3. Evidence for a recessive inheritance of Turcot's syndrome caused by compound heterozygous mutations within the PMS2 gene

4. Novel PMS2 Pseudogenes Can Conceal Recessive Mutations Causing a Distinctive Childhood Cancer Syndrome

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