Screening of the duplication 24 pb of ARX gene in Moroccan patients with X-linked Intellectual Disability

Screening of the duplication 24 pb of ARX gene in Moroccan patients with X-linked Intellectual Disability

Abstract Objective Intellectual Disability (ID) represents a neuropsychiatric disorder, which its etiopathogenesis remains insufficiently understood. Mutations in the Aristaless Related Homeobox gene (ARX) have been identified to cause syndromic and nonsyndromic (NS-ID). The most recurrent mutation...

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Bibliographic Details
Main Authors: Yousra Benmakhlouf, Renaud Touraine, Ines Harzallah, Zeineb Zian, Kaoutar Ben Makhlouf, Amina Barakat, Naima Ghailani Nourouti, Mohcine Bennani Mechita
Format: Article
Language:English
Published: BMC 2021-03-01
Series:BMC Research Notes
Subjects:
Duplication 24 pb
ARX
X-linked intellectual disability
Nonsyndromic ID
Morocco
Online Access:https://doi.org/10.1186/s13104-021-05526-7

Internet

https://doi.org/10.1186/s13104-021-05526-7

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