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Orphanet Journal of Rare Diseases logoLink to Orphanet Journal of Rare Diseases
. 2020 Mar 30;15:79. doi: 10.1186/s13023-020-1350-8

Correction to: Immunological features of patients affected by Barraquer-Simons syndrome

Fernando Corvillo 1,2,, Giovanni Ceccarini 3, Pilar Nozal 1,2,4, Silvia Magno 3, Caterina Pelosini 3, Sofía Garrido 1,2,4, Alberto López-Lera 1,2, Manuela Moraru 5, Carlos Vilches 5, Silvia Fornaciari 6, Sabrina Gabbriellini 6, Ferruccio Santini 3, David Araújo-Vilar 7, Margarita López-Trascasa 1,8
PMCID: PMC7106744  PMID: 32228621

Correction to: Orphanet J Rare Dis

https://doi.org/10.1186/s13023-019-1292-1

Following the publication of the original article [1], the authors requested to amend the Abstract and Discussion section as follows:

Abstract

“The HLA allele DRB1*11 was present in 54% of BSS patients, and the majority of them (31%) were positive for *11:03 (vs 1.3% in the general population)”

has been amended to read:

“The HLA allele DRB1*11 was present in 54% of BSS patients, and the majority of them (31%) were positive for *11:03 (vs 1.3% allelic frequency in the general population)”.

Discussion

“Although no HLA allele was shared by the majority of our patients, interestingly, the allele DRB1*11:03 were overrepresented in our cohort (31% vs 1.3% in the general population)”

has been amended to read:

“Although no HLA allele was shared by the majority of our patients, interestingly, the allele DRB1*11:03 were overrepresented in our cohort (31% carrier frequency vs 1.3% allelic frequency in the general population)”.

The correction was deemed necessary to prevent possible misinterpretation of data deriving from the bibliography used. The original article has also been updated as above.

Reference

  • 1.Corvillo, et al. Immunological features of patients affected by Barraquer-Simons syndrome. Orphanet J Rare Dis. 2020;15:9. doi: 10.1186/s13023-019-1292-1. [DOI] [PMC free article] [PubMed] [Google Scholar]

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