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

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Main Authors: María Caridad Duran-Lemarie, Luis Enrique Cano-Aguilar, Edmar Obed Benitez-Alonso, Dalia Cruz-Sotomayor, Uriel Villela-Segura, Hector Proy-Trujillo
Format: Article
Language:English
Published: Sociedade Brasileira de Dermatologia 2025-03-01
Series:Anais Brasileiros de Dermatologia
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962025000100701&lng=en&tlng=en
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author María Caridad Duran-Lemarie
Luis Enrique Cano-Aguilar
Edmar Obed Benitez-Alonso
Dalia Cruz-Sotomayor
Uriel Villela-Segura
Hector Proy-Trujillo
author_facet María Caridad Duran-Lemarie
Luis Enrique Cano-Aguilar
Edmar Obed Benitez-Alonso
Dalia Cruz-Sotomayor
Uriel Villela-Segura
Hector Proy-Trujillo
author_sort María Caridad Duran-Lemarie
collection DOAJ
format Article
id doaj-art-4e5ede0673234be8a57006c2c40c4527
institution OA Journals
issn 0365-0596
language English
publishDate 2025-03-01
publisher Sociedade Brasileira de Dermatologia
record_format Article
series Anais Brasileiros de Dermatologia
spelling doaj-art-4e5ede0673234be8a57006c2c40c45272025-08-20T02:08:40ZengSociedade Brasileira de DermatologiaAnais Brasileiros de Dermatologia0365-05962025-03-01100110.1016/j.abd.2023.01.010Vohwinkel syndrome with de novo heterozygous mutation in the GJB2 gene - c.175G>A (p. Gly59Ser)María Caridad Duran-Lemariehttps://orcid.org/0000-0003-2207-8477Luis Enrique Cano-Aguilarhttps://orcid.org/0000-0003-0710-5430Edmar Obed Benitez-Alonsohttps://orcid.org/0000-0002-3813-0359Dalia Cruz-Sotomayorhttps://orcid.org/0000-0002-3891-1390Uriel Villela-Segurahttps://orcid.org/0000-0002-6467-4691Hector Proy-Trujillohttps://orcid.org/0000-0002-8023-2148http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962025000100701&lng=en&tlng=en
spellingShingle María Caridad Duran-Lemarie
Luis Enrique Cano-Aguilar
Edmar Obed Benitez-Alonso
Dalia Cruz-Sotomayor
Uriel Villela-Segura
Hector Proy-Trujillo
Vohwinkel syndrome with de novo heterozygous mutation in the GJB2 gene - c.175G>A (p. Gly59Ser)
Anais Brasileiros de Dermatologia
title Vohwinkel syndrome with de novo heterozygous mutation in the GJB2 gene - c.175G>A (p. Gly59Ser)
title_full Vohwinkel syndrome with de novo heterozygous mutation in the GJB2 gene - c.175G>A (p. Gly59Ser)
title_fullStr Vohwinkel syndrome with de novo heterozygous mutation in the GJB2 gene - c.175G>A (p. Gly59Ser)
title_full_unstemmed Vohwinkel syndrome with de novo heterozygous mutation in the GJB2 gene - c.175G>A (p. Gly59Ser)
title_short Vohwinkel syndrome with de novo heterozygous mutation in the GJB2 gene - c.175G>A (p. Gly59Ser)
title_sort vohwinkel syndrome with de novo heterozygous mutation in the gjb2 gene c 175g a p gly59ser
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962025000100701&lng=en&tlng=en
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