Vohwinkel syndrome with de novo heterozygous mutation in the GJB2 gene - c.175G>A (p. Gly59Ser)
| Autor: | Duran-Lemarie, María Caridad a, Cano-Aguilar, Luis Enrique a, Benitez-Alonso, Edmar Obed b, Cruz-Sotomayor, Dalia c, Villela-Segura, Uriel d, Proy-Trujillo, Hector e, ⁎ |
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| Zdroj: | In Anais Brasileiros de Dermatologia January-February 2025 100(1):190-193 |
| Databáze: | ScienceDirect |
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