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The PTRHD1 Mutation in Intellectual Disability.

Sara CheraghiSahar MoghbelinejadHossein NajmabadiKimia KahriziReza Najafipour
Published 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.
Keyphrases
  • intellectual disability
  • autism spectrum disorder
  • copy number
  • parkinson disease
  • genome wide