Report of a novel missense mutation in the MECP2 gene in a middle-aged man with intellectual disability syndrome.
Maria ArvioMaria K HaanpääPia PohjolaJaana LähdetiePublished in: Clinical case reports (2021)
Exome sequencing revealed the cause of our 35-year-old male patient's progressive and severe intellectual and motor disability, namely a previously undescribed missense mutation of MECP2.