Elevated Fmr1 mRNA levels and reduced protein expression in a mouse model with an unmethylated Fragile X full mutation
Author:
Publisher
Elsevier BV
Subject
Cell Biology
Reference41 articles.
1. Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox;Fu;Cell,1991
2. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome;Verkerk;Cell,1991
3. Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the Fragile-X syndrome;Tassone;Am. J. Hum. Genet.,2000
4. Reduced FMRP and increased FMR1 transcription is proportionally associated with CGG repeat number in intermediate-length and premutation carriers;Kenneson;Hum. Mol. Genet.,2001
5. Premature ovarian failure among Fragile X premutation carriers: parent-of-origin effect?;Sherman;Am. J. Hum. Genet.,2000
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