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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Autors principals: 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
Idioma:Inglês
Publicat: 2012
Matèries:
Article
Accés en línia: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
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars