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 (FMR1) gene on the long arm of the X chromosome. Children with FXS are commonly co-diagnosed with Autism Spectrum Disorder, attention an...

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Detalles Bibliográficos
Autores principales: Protic, Dragana D., Aishworiya, Ramkumar, Salcedo-Arellano, Maria Jimena, Tang, Si Jie, Milisavljevic, Jelena, Mitrovic, Filip, Hagerman, Randi J., Budimirovic, Dejan B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8875233/
https://www.ncbi.nlm.nih.gov/pubmed/35216055
http://dx.doi.org/10.3390/ijms23041935

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8875233/
https://www.ncbi.nlm.nih.gov/pubmed/35216055
http://dx.doi.org/10.3390/ijms23041935

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