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

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 of this...

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Detalles Bibliográficos
Autores principales: Benmakhlouf, Yousra, Touraine, Renaud, Harzallah, Ines, Zian, Zeineb, Ben Makhlouf, Kaoutar, Barakat, Amina, Ghailani Nourouti, Naima, Bennani Mechita, Mohcine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research Note
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7988900/
https://www.ncbi.nlm.nih.gov/pubmed/33757564
http://dx.doi.org/10.1186/s13104-021-05526-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7988900/
https://www.ncbi.nlm.nih.gov/pubmed/33757564
http://dx.doi.org/10.1186/s13104-021-05526-7

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