Changes in expression of the long noncoding RNA FMR4 associate with altered gene expression during differentiation of human neural precursor cells

CGG repeat expansions in the Fragile X mental retardation 1 (FMR1) gene are responsible for a family of associated disorders characterized by either intellectual disability and autism (Fragile X Syndrome, FXS), or adult-onset neurodegeneration (Fragile X-associated Tremor/Ataxia Syndrome, FXTAS). Ho...

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Main Authors: Veronica Julia Peschansky, Chiara ePastori, Zane eZeier, Dario eMotti, Katya eWentzel, Dmitry eVelmeshev, Marco eMagistri, John L Bixby, Vance P Lemmon, José P Silva, Claes eWahlestedt
Format: Article
Language:English
Published: Frontiers Media S.A. 2015-08-01
Series:Frontiers in Genetics
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fgene.2015.00263/full