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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Bibliografiska uppgifter
Huvudupphovsmän: Papadopoulo, D, Guillouf, C, Mohrenweiser, H, Moustacchi, E
Materialtyp: Artigo
Språk:Inglês
Publicerad: 1990
Ämnen:
Research Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC54960/
https://ncbi.nlm.nih.gov/pubmed/2236046
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