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The mismatch repair protein MSH2 is rate-limiting for repeat expansion in a Fragile X premutation mouse model
Fragile X-associated tremor and ataxia syndrome, Fragile X-associated primary ovarian insufficiency and Fragile X syndrome are Repeat Expansion Diseases caused by expansion of a CGG•CCG-repeat microsatellite in the 5′ UTR of the FMR1 gene. To help understand the expansion mechanism responsible for t...
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| Hlavní autoři: | , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2014
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3951054/ https://ncbi.nlm.nih.gov/pubmed/24130133 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/humu.22464 |
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