COMPLEMENTATION OF HYPERSENSITIVITY TO DNA INTERSTRAND CROSSLINKING AGENTS DEMONSTRATES THAT XRCC2 IS A FANCONI ANEMIA GENE

BACKGROUND: Fanconi anemia (FA) is a heterogeneous inherited disorder clinically characterized by progressive bone marrow failure, congenital anomalies, and a predisposition to malignancies. OBJECTIVE: Determine, based on correction of cellular phenotypes, whether XRCC2 is a FA gene. METHODS: Cells...

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Detaylı Bibliyografya
Yayımlandı:J Med Genet
Asıl Yazarlar: Park, Jung-Young, Virts, Elizabeth L., Jankowska, Anna, Wiek, Constanze, Othman, Mohamed, Chakraborty, Sujata C., Vance, Gail H., Alkuraya, Fowzan S., Hanenberg, Helmut, Andreassen, Paul R.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2016
Konular:
Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5035190/
https://ncbi.nlm.nih.gov/pubmed/27208205
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmedgenet-2016-103847
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