Corrigendum #2 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

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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. 2021.

. 2021 Aug 28:2021:9897523.

doi: 10.1155/2021/9897523. eCollection 2021.

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. Jamie H. C., Rachel L., Rachel G., Tahnee N. C., Anna H., Natario L. C. Eye Manifestations of Shprintzen–Goldberg Craniosynostosis Syndrome: A Case Report and Systematic Review. Case Reports in Genetics. 2020;2020 doi: 10.1155/2020/7353452.7353452 - DOI - PMC - PubMed
1. LopezCourcet A. J., Doyle J. J., Bessling S. L., et al. Mutations in the TGF-β Repressor SKI Cause Shprintzen-Goldberg Syndrome with Aortic Aneurysm. Nature Genetics. 2012;44(11):1249–1254. - PMC - PubMed