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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

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