A point mutation in the nuclease domain of MLH3 eliminates repeat expansions in a mouse stem cell model of the Fragile X-related disorders
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Title
A point mutation in the nuclease domain of MLH3 eliminates repeat expansions in a mouse stem cell model of the Fragile X-related disorders
Authors
Keywords
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Journal
NUCLEIC ACIDS RESEARCH
Volume -, Issue -, Pages -
Publisher
Oxford University Press (OUP)
Online
2020-07-03
DOI
10.1093/nar/gkaa573
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Note: Only part of the references are listed.- Human MutLγ, the MLH1–MLH3 heterodimer, is an endonuclease that promotes DNA expansion
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