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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Detaylı Bibliyografya
Yayımlandı:Iran J Child Neurol
Asıl Yazarlar: ALEYASIN, Seyed ahmad, SALAMAT, Fatemeh, MIRAKHORI, Mojgan
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Shahid Beheshti University of Medical Sciences 2018
Konular:
Original Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5760672/
https://ncbi.nlm.nih.gov/pubmed/29379561
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