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Hunsaker, Michael R.; von Leden, Ramona E.; Ta, Binh T.; Goodrich-Hunsaker, Naomi J.; Arque, Gloria; Kim, Kyoungmi; Willemsen, Rob; Berman, Robert F. (2011)
Languages: English
Types: Article
Subjects: Article

Classified by OpenAIRE into

mesheuropmc: congenital, hereditary, and neonatal diseases and abnormalities, nervous system diseases
Identifiers:pmc:PMC3095688
The fragile X premutation is a tandem CGG trinucleotide repeat expansion on the FMR1 gene between 55 and 200 repeats in length. A CGG knock-in (CGG KI) mouse with CGG trinucleotide repeat lengths between 70 and 350 has been developed and used to model the histopathology and cognitive deficits reported in carriers of the fragile X premutation. Previous studies have shown that CGG KI mice show progressive deficits in processing spatial and temporal information. To characterize the motor deficits associated with the fragile X premutation, male and female CGG KI mice ranging from 2–16 months of age with trinucleotide repeats ranging from 72–240 CGG in length were tested for their ability to perform a skilled ladder rung walking test. The results demonstrate that both male and female CGG KI mice showed a greater number of foot slips as a function of increased CGG repeat length, independent of the age of the animal or general activity level.
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