Pubblicazioni

A novel autosomal recessive GJB2-associated disorder: Ichthyosis follicularis, bilateral severe sensorineural hearing loss, and punctate palmoplantar keratoderma

2019 - HUMAN MUTATION

Youssefian, L.; Vahidnezhad, H.; Saeidian, A. H.; Mahmoudi, H.; Karamzadeh, R.; Kariminejad, A.; Huang, J.; Li, L.; Jannace, T. F.; Fortina, P.; Zeinali, S.; White, T. W.; Uitto, J.