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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.
Kaiyrzhanov, Rauan and Rad, Aboulfazl and Lin, Sheng-Jia and Bertoli-Avella, Aida and W Kallemeijn, Wouter and Godwin, Annie (2024) Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders. Brain.
