Hypomutability in Fanconi anemia cells is associated with increased deletion frequency at the HPRT locus.

Fanconi anemia (FA) is an inherited human disorder associated with a predisposition to cancer and characterized by anomalies in the processing of DNA cross-links and certain monoadducts. We reported previously that the frequency of psoralen-photoinduced mutations at the HPRT locus is lower in FA cel...

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Pubblicato in:	Proc Natl Acad Sci U S A
Autori principali:	Papadopoulo, D, Guillouf, C, Mohrenweiser, H, Moustacchi, E
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	National Academy of Sciences 1990
Soggetti:	Research Article
Accesso online:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC54960/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2236046/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.87.21.8383
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