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Koparir, Asuman and Bahena Carbajal, Paulina and Zamini, Mina and Naghinejad, Maryam and Najarzadeh Torbati, Paria and Hofrichter, Michaela A. H. and Tovornik, Stefanie and Koparir, Erkan and Dragicevic Babic, Neda and Aboulfazl, Rad and Daniel, Owrang and Kalay, Irem and Chamanrou, Niloofar and Nicolás Martínez, Luis (2026) Clinical and genetic heterogeneity of syndromic hearing loss and its non-syndromic hearing loss mimics. Molecular Medicine.
Owrang, Daniel and Rad, Aboulfazl and Alerasool, Masoome and M. Kolb, Susanne and Lin, Sheng-Jia and Doll, Julia and Alidadiani, Neda and Ghaderi, Shahrooz and Hofrichter, Michaela A. H. and Maroofian, Reza and Varshney, Gaurav K. and Mojarrad, Majid and Bartsch, Oliver and Haaf, Thomas and Vona, Barbara (2025) Expansion of Molecular and Clinical Aspects of EPS8L2 (DFNB106)-Associated Hearing Loss Emphasizes a Potential Therapeutic Window. Molecular Neurobiology.
