Response to Yang et al
- PMID: 31043712
- DOI: 10.1038/s41436-019-0530-1
Response to Yang et al
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.
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How should we correctly interpret biallelic germline truncating variant of MLH3 in hereditary colorectal cancer?Genet Med. 2019 Nov;21(11):2650-2651. doi: 10.1038/s41436-019-0529-7. Epub 2019 May 2. Genet Med. 2019. PMID: 31043711 No abstract available.
References
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- Olkinuora A, Nieminen TT, Mårtensson E, et al. Biallelic germline nonsense variant of MLH3 underlies polyposis predisposition. Genet Med. 2018 Dec 21; https://doi.org/10.1038/s41436-018-0405-x [Epub ahead of print].
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- Yang M, Zhu L, Xu D, et al. Response to Olkinuora et al. 2018: How should we correctly interpret biallelic germline truncating variant of MLH3 in hereditary colorectal cancer? Genet Med. 2019; https://doi.org/10.1038/s41436-019-0529-7 [Epub ahead of print].
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- Jiricny J. Postreplicative mismatch repair. Cold Spring Harb Perspect Biol. 2013;5:a012633. - DOI
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- Goodenberger ML, Thomas BC, Riefert-Johnson D, et al. PMS2 monoallelic mutation carriers: the known unknown. Genet Med. 2016;18:13–19. - DOI
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- Levi Z, Kariv R, Barnes-Kedar I, et al. The gastrointestinal manifestation of constitutional mismatch repair deficiency syndrome: from a single adenoma to polyposis-like phenotype and early onset cancer. Clin Genet. 2015;88:474–478. - DOI
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