Haplotype Analysis of DXS548 and FRAXAC1 Microsatellite Loci in Iranian Patients with Fragile X Syndrome

OBJECTIVE: Fragile X syndrome (FXS) is the most common cause of inherited mental retardation caused by expansion of a (CGG) repeat region up to 1000 repeat in 5' region of the FMR1 gene located in FRAXA locus Xq27.3. To better understand the mechanism involved in expansion of CGG region, the mo...

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Publicado en:Iran J Child Neurol
Main Authors: ALEYASIN, Seyed ahmad, SALAMAT, Fatemeh, MIRAKHORI, Mojgan
Formato: Artigo
Idioma:Inglês
Publicado: Shahid Beheshti University of Medical Sciences 2018
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Original Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC5760672/
https://ncbi.nlm.nih.gov/pubmed/29379561
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