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Erschienen in: Orphanet Journal of Rare Diseases 1/2011

Open Access 01.12.2011 | Erratum

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

verfasst von: Chiara Redaelli, Rosalind A Coleman, Laura Moro, Amalia Sertedaki, Talia Kakourou, Solaf Mohamed Elsayed, Daniele Prati, Agostino Colli, Donatella Mela, Roberto Colombo, Daniela Tavian

Erschienen in: Orphanet Journal of Rare Diseases | Ausgabe 1/2011

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Hinweise
The online version of the original article can be found at 10.​1186/​1750-1172-5-33

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.

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.
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.

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.
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Literatur
1.
Zurück zum Zitat 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.PubMedCentralCrossRefPubMed 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.PubMedCentralCrossRefPubMed
Metadaten
Titel
Erratum To:Clinical and genetic characterization of chanarin-dorfman syndrome patients: first report of large deletions in the ABHD5 gene
verfasst von
Chiara Redaelli
Rosalind A Coleman
Laura Moro
Amalia Sertedaki
Talia Kakourou
Solaf Mohamed Elsayed
Daniele Prati
Agostino Colli
Donatella Mela
Roberto Colombo
Daniela Tavian
Publikationsdatum
01.12.2011
Verlag
BioMed Central
Erschienen in
Orphanet Journal of Rare Diseases / Ausgabe 1/2011
Elektronische ISSN: 1750-1172
DOI
https://doi.org/10.1186/1750-1172-6-6

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