Front. Neurosci. Frontiers in Neuroscience Front. Neurosci. 1662-453X Frontiers Media S.A. 10.3389/fnins.2023.1344915 Neuroscience Correction Corrigendum: Case report: A patient with Delayed Sleep-Wake Phase Disorder and Optic Nerve Hypoplasia treated with tasimelteon: a case study Smieszek Sandra P. 1 * Kaden Alyssa R. 1 Johnson Caroline E. 1 Brzezynski Jennifer L. 1 Xiao Changfu 1 Polymeropoulos Christos M. 1 Birznieks Gunther 1 Emsellem Helene A. 2 3 Polymeropoulos Mihael H. 1 1Vanda Pharmaceuticals Inc., Washington, DC, United States 2The Center for Sleep & Wake Disorders, Chevy Chase, MD, United States 3Department of Neurology, George Washington University, Washington, DC, United States

Edited and reviewed by: Melissa A. St. Hilaire, Merrimack College, United States

 *Correspondence: Sandra P. Smieszek sandra.smieszek@vandapharma.com 08 01 2024 2023 17 1344915 27 11 2023 18 12 2023 Copyright © 2024 Smieszek, Kaden, Johnson, Brzezynski, Xiao, Polymeropoulos, Birznieks, Emsellem and Polymeropoulos. 2024 Smieszek, Kaden, Johnson, Brzezynski, Xiao, Polymeropoulos, Birznieks, Emsellem and Polymeropoulos

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 A corrigendum on Case report: A patient with Delayed Sleep-Wake Phase Disorder and Optic Nerve Hypoplasia treated with tasimelteon: a case study by Smieszek, S. P., Kaden, A. R., Johnson, C. E., Brzezynski, J. L., Xiao, C., Polymeropoulos, C. M., Birznieks, G., Emsellem, H. A., and Polymeropoulos, M. H. (2023). Front. Neurosci. 17:1287514. doi: 10.3389/fnins.2023.1287514 biological rhythms circadian rhythm disorders clinical trials research sleep/wake mechanisms Delayed Sleep-Wake Phase Disorder delayed sleep night owl Optic Nerve Hypoplasia section-at-acceptance Sleep and Circadian Rhythms

In the published article, there was an error. (There was an omission).

A correction has been made to Discussion, Paragraph 4. This sentence previously stated:

“This participant is not a carrier of the variable number of tandem repeat (VNTR) PER34/4 genotype, associated with delayed sleep patterns, nor the CRY1 splicing variant (Patke et al., 2017). No other predicted loss-of-function mutations within circadian genes were identified.”

The corrected sentence appears below:

“This participant is not a carrier of the variable number of tandem repeat (VNTR) PER34/4 genotype, associated with delayed sleep patterns, nor the CRY1 splicing variant (Patke et al., 2017). This patient has been determined to carry two 5′ UTR region variants in the Atonal BHLH Transcription Factor 7 (ATOH7) gene known to be associated with ONH, rs61854782 and rs7916697. ATOH7 is expressed in retinal progenitor cells and has a crucial role in retinal ganglion cell development. No other predicted loss-of-function mutations within circadian genes were identified.”

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.

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 References Patke A. Murphy P. Onat O. Krieger A. Özçelik T. Campbell S. . (2017). Mutation of the human circadian clock gene CRY1 in familial delayed sleep phase disorder. Cell 169, 203–215.e1. 10.1016/j.cell.2017.03.02728388406