The PTRHD1 Mutation in Intellectual Disability.
Sara CheraghiSahar MoghbelinejadHossein NajmabadiKimia KahriziReza NajafipourPublished in: Archives of Iranian medicine (2021)
PTRHD1 has been recently introduced as a candidate ID and Parkinsonism causing gene. Our findings are in agreement with the clinical spectrum of PTRHD1 mutations; however, our affected individuals suffer from ID manifestations.