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Erratum To:Clinical and genetic characterization of chanarin-dorfman syndrome patients: first report of large deletions in the ABHD5 gene

Orphanet Journal of Rare Diseases volume 6, Article number: 6 (2011) Cite this article

The Original Article was published on 01 December 2010

Correction

Following the publication of this article [1], it was clarified that the clinical follow-up of one of CDS family described in the manuscript was performed by Dr. Amalia Sertedaki and Talia Kakourou. The authorship of the article has been changed accordingly. The submitting authors would like to apologise to Amalia Sertedaki and Talia Kakourou for this error and they would like to thank Catherine Dacou-Voutetakis for underlining the problem.

References

  1. Redaelli C, Coleman RA, Moro L, Dacou-Voutetakis C, Elsayed SM, Prati D, Colli A, Mela D, Colombo R, Tavian D: Clinical and genetic characterization of Chanarin-Dorfman Syndrome patients: first report of large deletions in the ABHD5 gene. Orphanet J Rare Dis. 2010, 5:33. 10.1186/1750-1172-5-33.

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Authors and Affiliations

  1. Department of Psychology, Catholic University of the Sacred Heart, Milan, Italy

    Chiara Redaelli & Daniela Tavian

  2. Department of Nutrition, University of North Carolina, Chapel Hill, NC, USA

    Rosalind A Coleman

  3. DiSCAFF Department, University of Piemonte Orientale, Novara, Italy

    Laura Moro

  4. Department of Paediatrics, Athens University, Greece

    Amalia Sertedaki & Talia Kakourou

  5. Medical Genetics Center, Korba, Cairo, Egypt

    Solaf Mohamed Elsayed

  6. Department of Transfusion Medicine and Hematology, Ospedale Alessandro Manzoni, Lecco, Italy

    Daniele Prati

  7. Center of Transfusion Medicine, Cellular Therapy and CryoBiology, IRCCS Foundation Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy

    Daniele Prati

  8. Department of Internal Medicine, Ospedale Alessandro Manzoni, Lecco, Italy

    Agostino Colli

  9. Department of Internal Medicine, Santa Corona Hospital, Pietra Ligure, Italy

    Donatella Mela

  10. Institute of Biochemistry and Clinical Biochemistry, Catholic University, Gemelli Hospital, Rome, Italy

    Roberto Colombo

Authors
  1. Chiara Redaelli
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  2. Rosalind A Coleman
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  3. Laura Moro
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  4. Amalia Sertedaki
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  5. Talia Kakourou
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  6. Solaf Mohamed Elsayed
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  7. Daniele Prati
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  8. Agostino Colli
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  9. Donatella Mela
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  10. Roberto Colombo
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  11. Daniela Tavian
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Corresponding author

Correspondence to Daniela Tavian.

Additional information

Competing interests

The authors declare that they have no competing interests.

Authors' contributions

CR carried out the molecular genetic studies and the interpretation of the results. RAC and LM made substantial contributions to interpretation of data and participated in manuscript preparation. AS, TK, SME, DP, AC and RC were involved in the clinical evaluation of patients and manuscript revision. DT made substantial contributions to conception, analysis and interpretation of data and drafted the manuscript. All authors read and approved the final manuscript.

The online version of the original article can be found at 10.1186/1750-1172-5-33

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Open Access This article is published under license to BioMed Central Ltd. This is an Open Access article is distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/2.0 ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Redaelli, C., Coleman, R.A., Moro, L. et al. Erratum To:Clinical and genetic characterization of chanarin-dorfman syndrome patients: first report of large deletions in the ABHD5 gene. Orphanet J Rare Dis 6, 6 (2011). https://doi.org/10.1186/1750-1172-6-6

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  • DOI: https://doi.org/10.1186/1750-1172-6-6

Orphanet Journal of Rare Diseases

ISSN: 1750-1172