M. Kharrat

Electroclinical and genetic profiling of Tunisian families with malformations of cortical development: report of novel DENND5A mutation, functional DYNC1H/DCX variants and structural correlates

Malformations of cortical development (MCD) are neurodevelopmental disorders arising from disrupted neuronal proliferation and migration during embryogenesis and represent a major cause of epilepsy and developmental impairment. Although numerous genes have been implicated, varian...