Identification of a novel NBN truncating mutation in a family with hereditary prostate cancer

Nibrin (NBN), located on chromosome 8q21 is a gene involved in DNA double-strand break repair that has been implicated in the rare autosomal recessive chromosomal instability syndrome known as Nijmegen Breakage Syndrome. NBS is characterized by specific physical characteristics (microcephaly and dys...

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Bibliografski detalji
Glavni autori: Zuhlke, Kimberly A, Ray, Anna M, Okoth, Linda A, Stoffel, Elena M, Robbins, Christiane M, Tembe, Waibov A, Salinas, Claudia A, Zheng, S Lilly, Xu, Jianfeng, Carpten, John D, Lange, Ethan M, Isaacs, William B, Cooney, Kathleen A
Format: Artigo
Jezik:Inglês
Izdano: 2012
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Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3485445/
https://ncbi.nlm.nih.gov/pubmed/22864661
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10689-012-9555-1
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