Cancer Risk of Heterozygotes With the NBN Founder Mutation
Author:
Publisher
Oxford University Press (OUP)
Subject
Cancer Research,Oncology
Link
http://academic.oup.com/jnci/article-pdf/99/24/1875/7689350/djm251.pdf
Reference31 articles.
1. Nijmegen breakage syndrome
2. Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome
3. The hMre11/hRad50 Protein Complex and Nijmegen Breakage Syndrome: Linkage of Double-Strand Break Repair to the Cellular DNA Damage Response
4. Positional cloning of the gene for Nijmegen breakage syndrome
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