Fragile X Syndrome: From Molecular Aspect to Clinical Treatment

Fragile X Syndrome: From Molecular Aspect to Clinical Treatment

Fragile X syndrome (FXS) is a neurodevelopmental disorder caused by the full mutation as well as highly localized methylation of the fragile X mental retardation 1 (<i>FMR1</i>) gene on the long arm of the X chromosome. Children with FXS are commonly co-diagnosed with Autism Spectrum Dis...

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Bibliographic Details
Main Authors: Dragana D. Protic, Ramkumar Aishworiya, Maria Jimena Salcedo-Arellano, Si Jie Tang, Jelena Milisavljevic, Filip Mitrovic, Randi J. Hagerman, Dejan B. Budimirovic
Format: Article
Language:English
Published: MDPI AG 2022-02-01
Series:International Journal of Molecular Sciences
Subjects:
fragile X syndrome
<i>FMR1</i> gene
FMRP
behavior problems
autism spectrum disorder
Online Access:https://www.mdpi.com/1422-0067/23/4/1935

Internet

https://www.mdpi.com/1422-0067/23/4/1935

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