Understanding the Molecular Basis of Fragile X Syndrome Using Differentiated Mesenchymal Stem Cells

OBJECTIVES: Fragile X syndrome (FXS) has been known as the most common cause of inherited intellectual disability and autism. This disease results from the loss of fragile X mental retardation protein expression due to the expansion of CGG repeats located on the 5’ untranslated region of the fragile...

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Detalles Bibliográficos
Autores principales: FAZELI, Zahra, GHADERIAN, Sayyed Mohammad Hossein, NAJMABADI, Hossein, OMRANI, Mir Davood
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shahid Beheshti University of Medical Sciences 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8753000/
https://www.ncbi.nlm.nih.gov/pubmed/35222660
http://dx.doi.org/10.22037/ijcn.v15i4.22070

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8753000/
https://www.ncbi.nlm.nih.gov/pubmed/35222660
http://dx.doi.org/10.22037/ijcn.v15i4.22070

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