Evaluating the role of MLH3 p.Ser1188Ter variant in inherited breast cancer predisposition
- PMID: 31686011
- PMCID: PMC7056660
- DOI: 10.1038/s41436-019-0694-8
Evaluating the role of MLH3 p.Ser1188Ter variant in inherited breast cancer predisposition
Conflict of interest statement
The authors declare no conflicts of interest.
Comment on
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Biallelic germline nonsense variant of MLH3 underlies polyposis predisposition.Genet Med. 2019 Aug;21(8):1868-1873. doi: 10.1038/s41436-018-0405-x. Epub 2018 Dec 21. Genet Med. 2019. PMID: 30573798 Free PMC article.
References
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- Bonadona V, Bonaiti B, Olschwang S, Grandjouan S, Huiart L, Longy M, Guimbaud R, Buecher B, Bignon YJ, Caron O, Colas C, Nogues C, et al. Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome. JAMA. 2011;305:2304–2310. doi: 10.1001/jama.2011.743. - DOI - PubMed
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