Carta científica
Paquioniquia congénita: nuevo caso asociado al gen KRT17
Congenital pachyonychia: A new case associated with the KRT17 gene
O. Micol-Martíneza, V. López-Gonzálezb,c, P.W. Garcia-Marcosa, T. Martínez-Menchónd, E. Guillén-Navarrob,c,
Autor para correspondencia
a Servicio de Pediatría, Hospital Clínico Universitario Virgen de la Arrixaca, Murcia, España
b Sección de Genética Médica, Servicio de Pediatría, Hospital Clínico Universitario Virgen de la Arrixaca, IMIB-Arrixaca, Murcia, España
c Grupo Clínico vinculado al Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III (ISCIII), Madrid, España
d Unidad de Dermatología Infantil, Servicio de Dermatología, Hospital Clínico Universitario Virgen de la Arrixaca, Murcia, España
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