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Cartas ‐ Caso clínico
Síndrome de Vohwinkel com mutação heterozigótica de novo no gene GJB2 c.175G>A (p. Gly59Ser)
María Caridad Duran‐Lemariea, Luis Enrique Cano‐Aguilara, Edmar Obed Benitez‐Alonsob, Dalia Cruz‐Sotomayorc, Uriel Villela‐Segurad, Hector Proy‐Trujilloe,
a Departamento de Dermatologia, General Hospital “Dr Manuel Gea González”, Cidade do México, México
b Departamento de Neurogenética, National Institute of Neurology “Manuel Velasco Suárez”, Cidade do México, México
c Departamento de Dermatologia, Central Hospital “Dr Ignacio Morones Prieto”, San Luis Potosí, México
d Consultor em Dermatologia, Hospital Lomas de San Luis. San Luis Potosí, México
e Departamento de Cirurgia Dermatológica. Dermatology Center of Yucatan, Mérida, México
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ISSN: 26662752
Original language: Portuguese
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