Corrigendum: PTCHD1 gene mutation/deletion: the cognitive-behavioral phenotyping of four case reports

Front Psychiatry. 2024 Feb 13:15:1375954. doi: 10.3389/fpsyt.2024.1375954. eCollection 2024.

¹ Child and Adolescent Neuropsychiatry Unit, Department of Neuroscience, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
² Laboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesù Children Hospital, IRCCS, Rome, Italy.
³ Department of Pediatrics and Human Development, College of Human Medicine, Michigan State University, East Lansing, MI, United States.
⁴ Neurology Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
⁵ Greenwood Genetic Center, Gregor Mendel Circle, Greenwood, SC, United States.
⁶ Unit of Muscular and Neurodegenerative Disorders, Unit of Developmental Neurology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
⁷ Genetics and Rare Diseases Research Division, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.

^# Contributed equally.

Abstract

[This corrects the article DOI: 10.3389/fpsyt.2023.1327802.].

Keywords: PTCHD1 gene; autism spectrum disorder; cognitive-behavioral phenotype; intellectual disability; rare genetic syndrome.