Parzefall, T., Frohne, A., Koenighofer, M., Kirchnawy, A., Streubel, B., Schoefer, C., . . . Lucas, T. (2017). Identification of a rare COCH mutation by whole-exome sequencing: Implications for personalized therapeutic rehabilitation in an Austrian family with non-syndromic autosomal dominant late-onset hearing loss. Wien Klin Wochenschr.

Parzefall, Thomas, Alexandra Frohne, Martin Koenighofer, Andreas Kirchnawy, Berthold Streubel, Christian Schoefer, Wolfgang Gstoettner, Klemens Frei, a Trevor Lucas. "Identification of A rare COCH Mutation By Whole-exome Sequencing: Implications for Personalized Therapeutic Rehabilitation in an Austrian Family With Non-syndromic Autosomal Dominant Late-onset Hearing Loss." Wien Klin Wochenschr 2017.

Parzefall, Thomas, et al. "Identification of A rare COCH Mutation By Whole-exome Sequencing: Implications for Personalized Therapeutic Rehabilitation in an Austrian Family With Non-syndromic Autosomal Dominant Late-onset Hearing Loss." Wien Klin Wochenschr 2017.