The molecular basis of the Fragile X syndrome

The molecular basis of the Fragile X syndrome

This analysis aimed to clarify the molecular basis of fragile X syndrome and explain the role of genetic material in the genetic disease's development and treatment. Fragile X syndrome is an X-linked mutation inheritance disorder. The mutated gene is called FMR-1. This is important for normal...

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Bibliographic Details
Main Author:	Harem Othman smail
Format:	Article
Language:	English
Published:	"Alexandru Ioan Cuza" University of Iași 2023-05-01
Series:	Journal of Experimental and Molecular Biology
Subjects:	X-linked intellectual, FMR-1 triplet expansion region, RNA-binding protein, X mutation, DNA methylation, and Gene therapy
Online Access:	http://www.jemb.bio.uaic.ro/index.php/jemb/article/view/80

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