Corrigendum to "Eye Manifestations of Shprintzen-Goldberg Craniosynostosis Syndrome: A Case Report and Systematic Review"

Jamie H Choi¹, Rachel Li², Rachel Gannaway², Tahnee N Causey², Anna Harrison³, Natario L Couser^{2

3

4}

Affiliations

¹ Virginia Commonwealth University School of Medicine, Richmond, VA, USA.
² Department of Human and Molecular Genetics, Division of Clinical Genetics, Virginia Commonwealth University School of Medicine, Richmond, VA, USA.
³ Department of Ophthalmology, Virginia Commonwealth University School of Medicine, Richmond, VA, USA.
⁴ Department of Pediatrics, Virginia Commonwealth University School of Medicine, Richmond, VA, USA.

Published Erratum

Jamie H Choi et al. Case Rep Genet. 2020.

. 2020 Nov 11:2020:4708976.

doi: 10.1155/2020/4708976. eCollection 2020.

Jamie H Choi¹, Rachel Li², Rachel Gannaway², Tahnee N Causey², Anna Harrison³, Natario L Couser^{2

3

4}

¹ Virginia Commonwealth University School of Medicine, Richmond, VA, USA.
² Department of Human and Molecular Genetics, Division of Clinical Genetics, Virginia Commonwealth University School of Medicine, Richmond, VA, USA.
³ Department of Ophthalmology, Virginia Commonwealth University School of Medicine, Richmond, VA, USA.
⁴ Department of Pediatrics, Virginia Commonwealth University School of Medicine, Richmond, VA, USA.

Abstract

[This corrects the article DOI: 10.1155/2020/7353452.].

Eye Manifestations of Shprintzen-Goldberg Craniosynostosis Syndrome: A Case Report and Systematic Review.
Choi JH, Li R, Gannaway R, Causey TN, Harrison A, Couser NL. Choi JH, et al. Case Rep Genet. 2020 Aug 19;2020:7353452. doi: 10.1155/2020/7353452. eCollection 2020. Case Rep Genet. 2020. PMID: 33628537 Free PMC article.

1. Choi J. H., Li R., Gannaway R., Causey T. N., Harrison A., Couser N. L. Eye manifestations of Shprintzen–Goldberg Craniosynostosis syndrome: a case report and systematic review. Case Reports in Genetics. 2020;2020:5. doi: 10.1155/2020/7353452.7353452 - DOI - PMC - PubMed