Children With Fragile X Syndrome Display a Switch Towards Fast Fibres in Their Recruitment Strategy During Gait.

Background: Fragile X Syndrome (FXS) is a genetic disorder caused by the lack of FMRP, a crucial protein for brain development and function. FMR1 mutations are categorized into premutation and full mutation (FXSFull), with somatic mosaicism (FXSMos) modulating the FXS phenotype. Recent studies ident...

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Publicado en:	Journal of Intellectual Disability Research Vol. 69; no. 7; pp. 582 - 592
Autores principales:	Spolaor, Fabiola, Beghetti, Federica, Piatkowska, Weronika, Guiotto, Annamaria, Polli, Roberta, Bettella, Elisa, Liani, Valentina, di Giorgio, Elisa, Sawacha, Zimi
Formato:	equations & formulas research tables/charts Journal Article
Publicado:	Wiley-Blackwell Jul2025
Acceso en línea:	Ver este registro en EBSCOhost