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International Journal of Oral Science logoLink to International Journal of Oral Science
. 2021 Nov 12;13:35. doi: 10.1038/s41368-021-00141-5

Correction: Analyses of oligodontia phenotypes and genetic etiologies

Mengqi Zhou 1,2,3, Hong Zhang 1, Heather Camhi 4,5, Figen Seymen 6, Mine Koruyucu 6, Yelda Kasimoglu 6, Jung-Wook Kim 7,8, Hera Kim-Berman 4, Ninna M R Yuson 9, Paul J Benke 10, Yiqun Wu 2,, Feng Wang 11, Yaqin Zhu 3, James P Simmer 1,, Jan C-C Hu 1
PMCID: PMC8590003  PMID: 34772917

Correction to: International Journal of Oral Science 10.1038/s41368-021-00135-3, published online 30 September 2021

Following publication of this article,1 it is noticed Table 2 in this article needs revision.

Table 2.

Frequencies of tooth absence (in percentage) among the study cases affected by PAX9, MSX1, WNT10A, WNT10B, AXIN2, EDA, EDAR, EDARADD, LRP6, KREMEN1, SMOC2, and PITX2 gene mutations

graphic file with name 41368_2021_141_Tab1_HTML.jpg

Please note that the same type of tooth absent in the right and left arches were pooled together for the calculation. Numbers in gold color represent the highest frequency and numbers in blue color represent the lowest frequency of tooth type absence in each causative gene Ca canine; CI central incisor; LI lateral incisor; Mo molar; PM premolar.

The correct Table 2 is provided in this Correction.

The original article has been updated.

Contributor Information

Yiqun Wu, Email: yiqunwu@hotmail.com.

James P. Simmer, Email: jsimmer@umich.edu

Reference

  • 1.Zhou M, Zhang H, Camhi H, et al. Analyses of oligodontia phenotypes and genetic etiologies. Int. J. Oral Sci. 2021;13:32. doi: 10.1038/s41368-021-00135-3. [DOI] [PMC free article] [PubMed] [Google Scholar]

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