How should we correctly interpret biallelic germline truncating variant of MLH3 in hereditary colorectal cancer?
- PMID: 31043711
- DOI: 10.1038/s41436-019-0529-7
How should we correctly interpret biallelic germline truncating variant of MLH3 in hereditary colorectal cancer?
Comment in
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Response to Yang et al.Genet Med. 2019 Nov;21(11):2652-2653. doi: 10.1038/s41436-019-0530-1. Epub 2019 May 2. Genet Med. 2019. PMID: 31043712 No abstract available.
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
Reference
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- Olkinuora A, 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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