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

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...

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Détails bibliographiques
Auteurs principaux: Scott, Richard H, Homfray, Tessa, Huxter, Nicola L, Mitton, Sally G, Nash, Ruth, Potter, Mike N, Lancaster, Donna, Rahman, Nazneen
Format: Artigo
Langue:Inglês
Publié: BMJ Group 2007
Sujets:
Online Mutation Report
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC2597999/
https://ncbi.nlm.nih.gov/pubmed/17601929
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2007.048942
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