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CORRECTION article

Front. Psychiatry, 13 February 2024
Sec. Intellectual Disabilities
Volume 15 - 2024 | https://doi.org/10.3389/fpsyt.2024.1375954

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

This article is a correction to:

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

    1. Read original article
Federica Alice Maria Montanaro&#x;Federica Alice Maria Montanaro1†Alessandra Mandarino&#x;Alessandra Mandarino1†Viola AlesiViola Alesi2Charles SchwartzCharles Schwartz3Daniela Judith Claps SepulvedaDaniela Judith Claps Sepulveda4Cindy SkinnerCindy Skinner5Michael FriezMichael Friez5Gabriele PiccoloGabriele Piccolo6Antonio NovelliAntonio Novelli2Ginevra ZanniGinevra Zanni6Maria Lisa DenticiMaria Lisa Dentici7Stefano VicariStefano Vicari1Paolo Alfieri*Paolo Alfieri1*
  • 1Child and Adolescent Neuropsychiatry Unit, Department of Neuroscience, Bambino Gesù Children’s Hospital, IRCCS, Rome, Italy
  • 2Laboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesù Children Hospital, IRCCS, Rome, Italy
  • 3Department of Pediatrics and Human Development, College of Human Medicine, Michigan State University, East Lansing, MI, United States
  • 4Neurology Unit, Bambino Gesù Children’s Hospital, IRCCS, Rome, Italy
  • 5Greenwood Genetic Center, Gregor Mendel Circle, Greenwood, SC, United States
  • 6Unit of Muscular and Neurodegenerative Disorders, Unit of Developmental Neurology, Bambino Gesù Children’s Hospital, IRCCS, Rome, Italy
  • 7Genetics and Rare Diseases Research Division, Bambino Gesù Children’s Hospital, IRCCS, Rome, Italy

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

By Montanaro FAM, Mandarino A, Alesi V, Schwartz C, Sepulveda DJC, Skinner C, Friez M, Piccolo G, Novelli A, Zanni G, Dentici ML, Vicari S and Alfieri P (2024) Front. Psychiatry. 14:1327802. doi: 10.3389/fpsyt.2023.1327802

Text Correction

In the published article, there was an error in the name of a Figure.

A correction has been made to the section “2.7 Cytogenetics and molecular cytogenetics”, subsection “2.7.1 ARRAY-CGH analysis”. This sentence previously stated:

“(Figure 3 upper panel, pedigree, and graphical representation of array-CGH data).”

The corrected sentence appears below:

“(Figure 1 upper panel, pedigree, and graphical representation of array-CGH data)”.

In the published article, there was an error in the name of another Figure.

A correction has been made to the section “2.7 Cytogenetics and molecular cytogenetics”, subsection “2.7.3 3D structure and multiple sequence alignment”. This sentence previously stated:

“The multiple sequence alignment of PTCHD1 protein among organisms around the sites of p.F626S was obtained with Clustal Omega3 (Figure 4 )”

The corrected sentence appears below:

“The multiple sequence alignment of PTCHD1 protein among organisms around the sites of p.F626S was obtained with Clustal Omega3 (Figure 3 )”

In the published article, there was an error in a sentence.

A correction has been made to the section “2.7 Cytogenetics and molecular cytogenetics”, subsection “2.7.3 3D structure and multiple sequence alignment”. This sentence previously stated:

“Molecular structures were rendered with PyMOL.”

The corrected sentence appears below:

“Molecular structures were rendered with PyMOL (Figure 4).”

In the published article, there was an error in the reference to a Figure.

A correction has been made to the section “Discussion”. This sentence previously stated:

“(Figure 4 lower panel, showing amino acid conservation of the phenylalanine 626 residue).”

The corrected sentence appears below:

“(Figure 3 lower panel, showing amino acid conservation of the phenylalanine 626 residue).”

The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

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

Citation: Montanaro FAM, Mandarino A, Alesi V, Schwartz C, Sepulveda DJC, Skinner C, Friez M, Piccolo G, Novelli A, Zanni G, Dentici ML, Vicari S and Alfieri P (2024) Corrigendum: PTCHD1 gene mutation/deletion: the cognitive-behavioral phenotyping of four case reports. Front. Psychiatry 15:1375954. doi: 10.3389/fpsyt.2024.1375954

Received: 24 January 2024; Accepted: 01 February 2024;
Published: 13 February 2024.

Approved by:

Frontiers Editorial Office, Frontiers Media SA, Switzerland

Copyright © 2024 Montanaro, Mandarino, Alesi, Schwartz, Sepulveda, Skinner, Friez, Piccolo, Novelli, Zanni, Dentici, Vicari and Alfieri. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Paolo Alfieri, paolo.alfieri@opbg.net

†These authors have contributed equally to this work

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.