In the published article, there was an error in Figure 2 pertaining to SNP2 and SNP3 and is limited to the last 3 lines shown under each of these SNPs. The corrected Figure 2 appears below.
In the published article, there was an error in the Results section, subsection “Association of SFTP SNP-SNP Interaction With RDS”, subsection “Three SNP model intergenic interactions”, where “SNP 3- 1059047” should be “SNP3- 1059057”.
This sentence previously stated:The corrected sentence appears below:“This figure depicts an interaction among three SNPs of SFTPA1 and SFTPA2. In this intergenic interaction, the additive effect of SNP1, rs17886395, G variant that codes for alanine interacts with SNP2 (rs1059047) and SNP3 (rs1059047) of SFTPA1 in a dominant effect.”
“This figure depicts an interaction among three SNPs of SFTPA1 and SFTPA2. In this intergenic interaction, the additive effect of SNP1, rs17886395, G variant that codes for alanine interacts with SNP2 (rs1059047) and SNP3 (rs1059057) of SFTPA1 in a dominant effect.”
The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.
Figure 2
Summary
Keywords
epistasis, neonatal, genetic variants, pulmonary, allele
Citation
Amatya S, Ye M, Yang L, Gandhi CK, Wu R, Nagourney B and Floros J (2022) Corrigendum: Single nucleotide polymorphisms interactions of the surfactant protein genes associated with respiratory distress syndrome susceptibility in preterm infants. Front. Pediatr. 10:1069526. doi: 10.3389/fped.2022.1069526
Received
14 October 2022
Accepted
03 November 2022
Published
30 November 2022
Approved by
Maria Elisabetta Baldassarre, University of Bari Aldo Moro, Italy
Volume
10 - 2022
Updates
Copyright
© 2022 Amatya, Ye, Yang, Gandhi, Wu, Nagourney and Floros.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Joanna Floros jfloros@pennstatehealth.psu.edu
Specialty Section: This article was submitted to Genetics of Common and Rare Diseases, a section of the journal Frontiers in Pediatrics
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