Letter - Clinical
Vohwinkel syndrome with De novo mutation in the GJB2 gene with Heterozygous mutation c.175G>A (p. Gly59Ser)
María Caridad Duran-Lemariea, Luis Enrique Cano-Aguilara, Edmar Obed Benitez-Alonsob, Dalia Cruz-Sotomayorc, Ulises Villela-Segurad, Hector Proy-Trujilloe,
Corresponding author
a Department of Dermatology, General Hospital “Dr Manuel Gea González”, Mexico City, Mexico
b Department of Neurogenetics, National Institute of Neurology “Manuel Velasco Suárez”, Mexico City, Mexico
c Department of Dermatology, Central Hospital “Dr Ignacio Morones Prieto”, San Luis Potosí, Mexico
d Dermatology Consultant, Hospital Lomas de San Luis, San Luis Potosí, Mexico
e Deparment of Dermatologic Surgery, Dermatology Center of Yucatan, Mérida, Mexico
