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Familial T‐cell non‐Hodgkin lymphoma caused by biallelic MSH2 mutations

By Richard H Scott, Tessa Homfray, Nicola L Huxter, Sally G Mitton, Ruth Nash, Mike N Potter, Donna Lancaster and Nazneen Rahman

Abstract

Familial non‐Hodgkin lymphoma (NHL) is rare and in most cases, no underlying cause is identifiable. We report homozygous truncating mutations in the mismatch repair gene MSH2 (226C→T; Q76X) in three siblings who each developed T‐cell NHL in early childhood. All three children had hyperpigmented and hypopigmented skin lesions

Topics: Online Mutation Report
Publisher: BMJ Group
OAI identifier: oai:pubmedcentral.nih.gov:2597999
Provided by: PubMed Central
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