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

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Source: Human Mutation - November 15, 2018 Category: Genetics & Stem Cells Authors: Leila Youssefian, Hassan Vahidnezhad, Amir Hossein Saeidian, Hamidreza Mahmoudi, Razieh Karamzadeh, Ariana Kariminejad, Jianhe Huang, Leping Li, Thomas F. Jannace, Paolo Fortina, Sirous Zeinali, Thomas W. White, Jouni Uitto Tags: RESEARCH ARTICLE Source Type: research