Amina Barakat

Genetic Screening for Expanded FMR1 Alleles in a Moroccan Cohort With Unexplained Intellectual Disability

ABSTRACT Background Intellectual disability (ID) constitutes a major neurodevelopmental disorder (NDD), arising from diverse genetic and environmental aetiologies. Fragile X syndrome (FXS), caused by CGG repeat expansion in the FMR1 gene, is one of the most common inherited cause...