Massively parallel functional testing of MSH2 missense variants conferring Lynch syndrome risk.

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Bibliographic Details
Title: Massively parallel functional testing of MSH2 missense variants conferring Lynch syndrome risk.
Authors: Jia X; Department of Human Genetics, University of Michigan, Ann Arbor, MI 48109, USA., Burugula BB; Department of Human Genetics, University of Michigan, Ann Arbor, MI 48109, USA., Chen V; Department of Human Genetics, University of Michigan, Ann Arbor, MI 48109, USA., Lemons RM; Department of Human Genetics, University of Michigan, Ann Arbor, MI 48109, USA., Jayakody S; Department of Human Genetics, University of Michigan, Ann Arbor, MI 48109, USA., Maksutova M; Department of Human Genetics, University of Michigan, Ann Arbor, MI 48109, USA., Kitzman JO; Department of Human Genetics, University of Michigan, Ann Arbor, MI 48109, USA; Department of Computational Medicine & Bioinformatics, University of Michigan, Ann Arbor, MI 48109, USA. Electronic address: kitzmanj@umich.edu.
Source: American journal of human genetics [Am J Hum Genet] 2021 Jan 07; Vol. 108 (1), pp. 163-175. Date of Electronic Publication: 2020 Dec 23.
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1537-6605 (Electronic) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1537-6605
DOI:10.1016/j.ajhg.2020.12.003