Correction
Correction:Clinical and genetic characterization of chanarin-dorfman syndrome patients: first report of large deletions in the ABHD5 gene
1 Department of Psychology, Catholic University of the Sacred Heart, Milan, Italy
2 Department of Nutrition, University of North Carolina, Chapel Hill, NC, USA
3 DiSCAFF Department, University of Piemonte Orientale, Novara, Italy
4 Department of Paediatrics, Athens University, Greece
5 Medical Genetics Center, Korba, Cairo, Egypt
6 Department of Transfusion Medicine and Hematology, Ospedale Alessandro Manzoni, Lecco, Italy
7 Center of Transfusion Medicine, Cellular Therapy and CryoBiology, IRCCS Foundation Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy
8 Department of Internal Medicine, Ospedale Alessandro Manzoni, Lecco, Italy
9 Department of Internal Medicine, Santa Corona Hospital, Pietra Ligure, Italy
10 Institute of Biochemistry and Clinical Biochemistry, Catholic University, Gemelli Hospital, Rome, Italy
Orphanet Journal of Rare Diseases 2011, 6:6 doi:10.1186/1750-1172-6-6
Published: 21 February 2011First paragraph (this article has no abstract)
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.
