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Correction: Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients

Orphanet Journal of Rare Diseases volume 18, Article number: 190 (2023) Cite this article

The Original Article was published on 05 July 2023

Correction : Orphanet Journal of Rare Diseases (2023) 18:177 https://doi.org/10.1186/s13023-023-02780-9

Following publication of the original article [1], we have been notified that the sentence on equal contribution of the first authors was missed. It should be as follows:

Ali Zare Dehanavi and Maryam Bemanalizadeh have contributed equally to this work.

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Authors and Affiliations

  1. Department of Pediatrics, Division of Pediatric Neurology, Children’s Medical Center, Pediatrics Center of Excellence, Tehran University of Medical Sciences, Tehran, Iran

    Ali Zare Dehnavi, Maryam Bemanalizadeh, Mahmoud Reza Ashrafi, Morteza Heidari, Sareh Hosseinpour, Behnam Amini, Zahra Rezaei & Ali Reza Tavasoli

  2. Child Growth and Development Research Center, Research Institute for Primordial Prevention of Non-Communicable Disease, Isfahan University of Medical Sciences, Isfahan, Iran

    Maryam Bemanalizadeh

  3. Faculty of Medical Sciences, Department of Medical Genetics, Tarbiat Modares University, Tehran, Iran

    Seyyed Mohammad Kahani, Pouria Mohammadi & Masoud Garshasbi

  4. Skull Base Research Center, The Five Senses Health Institute, Rasoul Akram Hospital, Iran University of Medical Sciences, Tehran, Iran

    Mohammad Rohani

  5. Department of Neurology, Rasoul Akram Hospital, Iran University of Medical Sciences, Tehran, Iran

    Mohammad Rohani

  6. Department of Pediatrics, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran

    Mehran Beiraghi Toosi

  7. Neuroscience Research Center, Mashhad University of Medical Sciences, Mashhad, Iran

    Mehran Beiraghi Toosi

  8. Dr. Farhud’s Genetic Clinic, Tehran, Iran

    Shaghayegh Zokaei & Hajar Aryan

  9. School of Advanced Medical Science, Islamic Azad University, Tehran, Iran

    Shaghayegh Zokaei

  10. National Institute of Genetic Engineering and Biotechnology, Tehran, Iran

    Hajar Aryan

  11. Department of Neurology, Johns Hopkins Medicine, Baltimore, MD, USA

    Man Amanat

  12. Jefferson Institute of Molecular Medicine, Thomas Jefferson University, Philadelphia, PA, USA

    Hassan Vahidnezhad & Ali Reza Tavasoli

  13. Department of Dermatology and Cutaneous Biology, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, PA, USA

    Hassan Vahidnezhad

  14. Pediatric Neurology Division, Children’s Medical Center, Pediatrics Center of Excellence, Ataxia Clinic, Tehran University of Medical Sciences, Tehran, Iran

    Pouria Mohammadi & Ali Reza Tavasoli

Authors
  1. Ali Zare Dehnavi
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  2. Maryam Bemanalizadeh
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  3. Seyyed Mohammad Kahani
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  4. Mahmoud Reza Ashrafi
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  5. Mohammad Rohani
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  6. Mehran Beiraghi Toosi
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  7. Morteza Heidari
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  8. Sareh Hosseinpour
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  9. Behnam Amini
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  10. Shaghayegh Zokaei
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  11. Zahra Rezaei
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  12. Hajar Aryan
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  13. Man Amanat
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  14. Hassan Vahidnezhad
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  15. Pouria Mohammadi
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  16. Masoud Garshasbi
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  17. Ali Reza Tavasoli
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Corresponding authors

Correspondence to Masoud Garshasbi or Ali Reza Tavasoli.

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Dehnavi, A.Z., Bemanalizadeh, M., Kahani, S.M. et al. Correction: Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients. Orphanet J Rare Dis 18, 190 (2023). https://doi.org/10.1186/s13023-023-02794-3

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  • DOI: https://doi.org/10.1186/s13023-023-02794-3

Orphanet Journal of Rare Diseases

ISSN: 1750-1172