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Vohwinkel syndrome with de novo heterozygous mutation in the GJB2 gene - c.175G>A (p. Gly59Ser)

Published Print: 2025-01

Authors

Duran-Lemarie, María Caridad https://orcid.org/0000-0003-2207-8477
Cano-Aguilar, Luis Enrique https://orcid.org/0000-0003-0710-5430
Benitez-Alonso, Edmar Obed https://orcid.org/0000-0002-3813-0359
Cruz-Sotomayor, Dalia https://orcid.org/0000-0002-3891-1390
Villela-Segura, Uriel https://orcid.org/0000-0002-6467-4691
Proy-Trujillo, Hector https://orcid.org/0000-0002-8023-2148
Funding

Funding for this research was provided by:

Invitae (CA 94103, 05D2040778)
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Text and Data Mining valid from 2025-01-01

Text and Data Mining valid from 2025-01-01

Version of Record valid from 2024-10-19
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This article is maintained by: Elsevier

Article Title: Vohwinkel syndrome with de novo heterozygous mutation in the GJB2 gene - c.175G>A (p. Gly59Ser)

Journal Title: Anais Brasileiros de Dermatologia

CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.abd.2023.01.010

Content Type: article

Copyright: © 2024 Published by Elsevier España, S.L.U. on behalf of Sociedade Brasileira de Dermatologia.

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