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Elevated Levels of FMR1 mRNA in Carrier Males: A New Mechanism of Involvement in the Fragile-X Syndrome

The American Journal of Human Genetics · 2000 · Vol. 66(1) · pp. 6–15
Flora TassoneRandi J. HagermanAnnette K. TaylorLouise W. GaneTony E. GodfreyPaul J. Hagerman
Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder ResearchGenomic variations and chromosomal abnormalitiesFMR1Fragile X syndromeTrinucleotide repeat expansionGene silencingAlleleBiologyGeneGeneticsMessenger RNATranscription (linguistics)

MeSH terms

Fragile X SyndromeHeterozygoteHumansLeukocytesMaleNerve Tissue ProteinsRNA, MessengerSex FactorsRNA-Binding ProteinsTrinucleotide Repeat ExpansionReverse Transcriptase Polymerase Chain ReactionFragile X Messenger Ribonucleoprotein 1Fragile X Mental Retardation Protein
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767
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99%
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Elevated Levels of FMR1 mRNA in Carrier Males: A New Mechanism of Involvement in the Fragile-X Syndrome · Scinovex