Corrigendum #2 to “Eye Manifestations of Shprintzen–Goldberg Craniosynostosis Syndrome: A Case Report and Systematic Review”-Reference-Cited by-同舟云学术

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Corrigendum #2 to “Eye Manifestations of Shprintzen–Goldberg Craniosynostosis Syndrome: A Case Report and Systematic Review”

Published:2021-08-28 Issue: Volume:2021 Page:1-2
ISSN:2090-6552
Container-title:Case Reports in Genetics
language:en
Short-container-title:Case Reports in Genetics

Author:

Choi Jamie H.¹^ORCID,Li Rachel²,Gannaway Rachel²,Causey Tahnee N.²,Harrison Anna³,Couser Natario L.²³⁴^ORCID

Affiliation:

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

Publisher

Hindawi Limited

Subject

General Medicine

Link

http://downloads.hindawi.com/journals/crig/2021/9897523.pdf

Reference2 articles.

1. Eye Manifestations of Shprintzen–Goldberg Craniosynostosis Syndrome: A Case Report and Systematic Review

2. Mutations in the TGF-β Repressor SKI Cause Shprintzen-Goldberg Syndrome with Aortic Aneurysm;A. J. LopezCourcet;Nature Genetics,2012

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