Serum matrix metalloproteinase-9 (MMP9) and amyloid-beta protein precursor (APP) as potential biomarkers in children with Fragile-X syndrome: A cross sectional study

Author:

Bekheet Mohamed H.Y.,Mansour Lamiaa A.,Elkaffas Rasha H.,Kamel Mona A.,Elmonem Mohamed A.

Funder

Cairo University

Publisher

Elsevier BV

Subject

Clinical Biochemistry,General Medicine

Reference46 articles.

1. An “Omic” Overview of Fragile X Syndrome;Dionne;Biology,2021

2. Fragile X syndrome: clinical presentation, pathology and treatment;Salcedo-Arellano;Gac. Med. Mex.,2020

3. EMQN best practice guidelines for the molecular genetic testing and reporting of fragile X syndrome and other fragile X-associated disorders;Biancalana;Eur. J. Hum. Genet.,2015

4. Fragile X syndrome: Current insight;Dean;Egypt. J. Med. Hum. Genet.,2016

5. Co-occurring conditions associated with FMR1 gene variations: findings from a national parent survey;Bailey;Am. J. Med. Genet. Part A,2008

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