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Evaluating the role of NTHL1 p.Q90* allele in inherited breast cancer predisposition
BACKGROUND: Rare protein truncating variants of NTHL1 gene are causative for the recently described, recessively inherited NTHL1 tumor syndrome that is characterized by an increased lifetime risk for colorectal cancer, colorectal polyposis, and breast cancer. Although there is strong evidence for br...
Autores principales: | Kumpula, Timo, Tervasmäki, Anna, Mantere, Tuomo, Koivuluoma, Susanna, Huilaja, Laura, Tasanen, Kaisa, Winqvist, Robert, de Voer, Richarda M., Pylkäs, Katri |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7667375/ https://www.ncbi.nlm.nih.gov/pubmed/32949222 http://dx.doi.org/10.1002/mgg3.1493 |
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