NDLI: Predictive functional assay-based classification of PMS2 variants in Lynch syndrome.

Content Provider	Europe PMC
Author	Rayner, Emily Tiersma, Yvonne Fortuno, Cristina van Hees‐Stuivenberg, Sandrine Drost, Mark Thompson, Bryony Spurdle, Amanda B. de Wind, Niels
Related Links	https://europepmc.org/backend/ptpmcrender.fcgi?accid=PMC9545740&blobtype=pdf
Page Count	10
ISSN	10597794
Journal	Human Mutation [Hum Mutat]
Volume Number	43
DOI	10.1002/humu.24387
PubMed Central reference number	PMC9545740
Issue Number	9
PubMed reference number	35451539
e-ISSN	10981004
Language	English
Publisher	John Wiley and Sons Inc.
Publisher Date	2022-04-28
Publisher Place	Hoboken
Access Restriction	Open
Rights License	This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. © 2022 The Authors. Human Mutation published by Wiley Periodicals LLC.
Subject Keyword	diagnostic assessment DNA mismatch repair functional analysis‐based classification Lynch syndrome PMS2 variants of uncertain significance
Content Type	Text
Resource Type	Article
Subject	Genetics Genetics (clinical)

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