Open Access

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

  • Chiara Redaelli1,
  • Rosalind A Coleman2,
  • Laura Moro3,
  • Amalia Sertedaki4,
  • Talia Kakourou4,
  • Solaf Mohamed Elsayed5,
  • Daniele Prati6, 7,
  • Agostino Colli8,
  • Donatella Mela9,
  • Roberto Colombo10 and
  • Daniela Tavian1Email author
Orphanet Journal of Rare Diseases20116:6

DOI: 10.1186/1750-1172-6-6

Received: 15 February 2011

Accepted: 21 February 2011

Published: 21 February 2011

The original article was published in Orphanet Journal of Rare Diseases 2010 5:33

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.

Notes

Declarations

Authors’ Affiliations

(1)
Department of Psychology, Catholic University of the Sacred Heart
(2)
Department of Nutrition, University of North Carolina
(3)
DiSCAFF Department, University of Piemonte Orientale
(4)
Department of Paediatrics, Athens University
(5)
Medical Genetics Center
(6)
Department of Transfusion Medicine and Hematology, Ospedale Alessandro Manzoni
(7)
Center of Transfusion Medicine, Cellular Therapy and CryoBiology, IRCCS Foundation Ca' Granda Ospedale Maggiore Policlinico
(8)
Department of Internal Medicine, Ospedale Alessandro Manzoni
(9)
Department of Internal Medicine, Santa Corona Hospital
(10)
Institute of Biochemistry and Clinical Biochemistry, Catholic University, Gemelli Hospital

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.PubMed CentralView ArticlePubMedGoogle Scholar

Copyright

© Redaelli et al; licensee BioMed Central Ltd. 2011

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://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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