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Correction to: A complex pheotype in a girl with a novel heterozygous missense variant (p.Ile56Phe) of the GNAS gene

Orphanet Journal of Rare Diseases volume 17, Article number: 169 (2022) Cite this article

The Original Article was published on 23 February 2022

Correction to: Orphanet Journal of Rare Diseases (2022) 17:83 https://doi.org/10.1186/s13023-022-02252-6

Following the publication of the original article [1] we were informed that several of the co-authors’ given and family names had unfortunately been interchanged.

The correct author names are shown here below:

Paolo Cavarzere, Andrea Gastaldi, Francesca Marta Elli, Rossella Gaudino, Erika Peverelli, Milena Brugnara, Susanne Thiele, Francesca Granata, Giovanna Mantovani and Franco Antoniazzi

The author names have been corrected in the author list of this Correction and updated in the original article.

Reference

  1. Paolo C, et al. A complex pheotype in a girl with a novel heterozygous missense variant (p.Ile56Phe) of the GNAS gene. Orphanet J Rare Dis. 2022;17:83. https://doi.org/10.1186/s13023-022-02252-6.

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Authors and Affiliations

  1. Pediatric Division, Department of Pediatrics, University Hospital of Verona, Piazzale Stefani 1, 37126, Verona, Italy

    Paolo Cavarzere, Andrea Gastaldi, Rossella Gaudino, Milena Brugnara & Franco Antoniazzi

  2. Endocrinology Unit, Department of Clinical Sciences and Community Health, University of Milan, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Milan, Italy

    Francesca Marta Elli, Erika Peverelli & Giovanna Mantovani

  3. Pediatric Clinic, Department Surgical Sciences, Dentistry, Gynecology and Pediatrics, University of Verona, Verona, Italy

    Rossella Gaudino & Franco Antoniazzi

  4. Division of Paediatric Endocrinology and Diabetes, Department of Pediatrics, University of Lübeck, Luebeck, Germany

    Susanne Thiele

  5. General Medicine Unit, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Milan, Italy

    Francesca Granata

  6. Regional Center for the Diagnosis and Treatment of Children and Adolescents Rare Skeletal Disorders, Pediatric Clinic, Department of Surgical Sciences, Dentistry, Gynecology and Pediatrics, University of Verona, Verona, Italy

    Franco Antoniazzi

Authors
  1. Paolo Cavarzere
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  2. Andrea Gastaldi
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  3. Francesca Marta Elli
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  4. Rossella Gaudino
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  5. Erika Peverelli
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  6. Milena Brugnara
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  7. Susanne Thiele
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  8. Francesca Granata
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  9. Giovanna Mantovani
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  10. Franco Antoniazzi
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Corresponding author

Correspondence to Paolo Cavarzere.

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Cavarzere, P., Gastaldi, A., Elli, F.M. et al. Correction to: A complex pheotype in a girl with a novel heterozygous missense variant (p.Ile56Phe) of the GNAS gene. Orphanet J Rare Dis 17, 169 (2022). https://doi.org/10.1186/s13023-022-02316-7

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  • DOI: https://doi.org/10.1186/s13023-022-02316-7

Orphanet Journal of Rare Diseases

ISSN: 1750-1172