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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Dettagli Bibliografici
Autori principali: Scott, Richard H, Homfray, Tessa, Huxter, Nicola L, Mitton, Sally G, Nash, Ruth, Potter, Mike N, Lancaster, Donna, Rahman, Nazneen
Natura: Artigo
Lingua:Inglês
Pubblicazione: BMJ Group 2007
Soggetti:
Online Mutation Report
Accesso online: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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