 | Up a level |
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.
Koparir, Asuman and Lekszas, Caroline and Keseroglu, Kemal and Rose, Thalia and Rappl, Lena and Rad, Aboulfazl and Maroofian, Reza and Narendran, Nakul and Hasanzadeh, Atefeh and Ghayoor Karimiani, Ehsan and Boschann, Felix and Kornak, Uwe and Klopocki, Eva and Vona, Barbara and Haaf, Thomas and Liedtke, Daniel (2024) Zebrafish as a model to investigate a biallelic gain-of-function variant in MSGN1, associated with a novel skeletal dysplasia syndrome. Human Genomics.
