Fragile X Syndrome and FMR1 premutation: results from a survey on associated conditions and treatment priorities in Italy. [PDF]
Montanaro FAM +8 more
europepmc +1 more source
Cognitive dysfunction in women with the <i>FMR1</i> premutation during midlife: The LASSI-L reveals curvilinear CGG-dependent risk buffered by college education. [PDF]
Klusek J +5 more
europepmc +1 more source
Social Communication Delay in an Unbiased Sample of Preschoolers With the FMR1 Premutation. [PDF]
Klusek J +8 more
europepmc +1 more source
Reduced Sensorimotor, Working Memory, and Episodic Memory Abilities in Aging Female <i>FMR1</i> Premutation Carriers with and Without Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS). [PDF]
McGatlin K +10 more
europepmc +1 more source
The premutation of the fragile X messenger ribonucleoprotein 1 (FMR1) gene is characterized by an expansion of the CGG trinucleotide repeats (55 to 200 CGGs) in the 5’ untranslated region and increased levels of FMR1 mRNA. Molecular mechanisms leading to
Randi J. Hagerman +2 more
exaly +3 more sources
Preliminary Evidence of an Effect of Cerebellar Volume on Postural Sway in FMR1 Premutation Males [PDF]
Recent evidence suggests that early changes in postural control may be discernible among females with premutation expansions (55-200 CGG repeats) of the fragile X mental retardation 1 (FMR1) gene at risk of developing fragile X-associated tremor ataxia ...
Rachael Cvejic +2 more
exaly +2 more sources
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