The NBN founder mutation—Evidence for a country specific difference in age at cancer manifestation

BACKGROUND: Nijmegen breakage syndrome (NBS) is an autosomal‐recessive chromosome instability disorder characterized by, among others, hypersensitivity to X‐irradiation and an exceptionally high risk for lymphoid malignancy. The vast majority of NBS patients is homozygous for a common Slavic founder...

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Detalles Bibliográficos
Autores principales: Chrzanowska, Krystyna H., Seemanova, Eva, Varon, Raymonda, Digweed, Martin, Piekutowska‐Abramczuk, Dorota, Sperling, Karl, Seeman, Pavel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9939984/
https://www.ncbi.nlm.nih.gov/pubmed/36806726
http://dx.doi.org/10.1002/cnr2.1700

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9939984/
https://www.ncbi.nlm.nih.gov/pubmed/36806726
http://dx.doi.org/10.1002/cnr2.1700

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