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CTNNB1 gene mutation associated with neurodevelopmental disorder, microcephaly, and persistence of bilateral hyperplastic primary vitreous: A case report and literature review

Crossref DOI link: https://doi.org/10.1016/j.oftale.2020.11.018

Published Print: 2022-01

Update policy: https://doi.org/10.1016/elsevier_cm_policy

Authors

Zuluaga Gómez, L.M.

Caballero Mojica, S.C.

Vélez Rengifo, G.J.

Bravo Acosta, J.D.

Montoya Villada, J.H.
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Article Title: CTNNB1 gene mutation associated with neurodevelopmental disorder, microcephaly, and persistence of bilateral hyperplastic primary vitreous: A case report and literature review

Journal Title: Archivos de la Sociedad Española de Oftalmología (English Edition)

CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.oftale.2020.11.018

CrossRef DOI link to the associated document: https://doi.org/10.1016/j.oftal.2020.11.028

Content Type: simple-article

Copyright: © 2021 Sociedad Española de Oftalmología. Published by Elsevier España, S.L.U. All rights reserved.

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