<i>FRMPD4</i> , a causal gene for intellectual disability and epilepsy, is associated with X-linked non-syndromic hearing loss

Daniel Liedtke(University of Würzburg), Barbara Vona(Brigham and Women's Hospital), Renske Schellens(Radboud University Nijmegen), Julia Doll(University of Würzburg), Oliver Bartsch(Johannes Gutenberg University Mainz), Katrina M. Schrode(Johns Hopkins University), Philip Hehlert(University of Göttingen), Erwin van Wijk(Radboud University Nijmegen), Amanda M. Lauer(Johns Hopkins University), Radoslaw Katana(University of Göttingen), Cordula Neuner, Marcus Dittrich(University of Würzburg), Wafaa Shehata-Dieler, K Rak(Universitätsklinikum Würzburg), Ulrich Zechner(Johannes Gutenberg University Mainz), Linda Bieniussa, T Wang(Johns Hopkins University), Niloofar Chamanrou(Shahrekord University), Mei Han, Indrajit Nanda(University of Würzburg), Johannes Voelker(Universitätsklinikum Würzburg), Lukas Jürgens(Universitätsklinikum Würzburg), Daniel Bengl(University of Würzburg), Eva Klopocki(University of Würzburg), Stefan Herms(University of Bonn), Hamid Galehdari(Shahid Chamran University of Ahvaz), Per Hoffmann(University of Bonn), Martin C Goepfert(University of Göttingen), Michaela AH Hofrichter(University of Würzburg), Peter M Krawitz(University of Bonn), Reza Maroofian(Wellcome Centre for Human Neuroimaging), Thomas Haaf(University of Würzburg), Soganad Heydaran(Shahid Chamran University of Ahvaz), Paul F Worley(Johns Hopkins University), Jörg Schröder(Dartmouth–Hitchcock Medical Center), Erik de Vrieze(Radboud University Nijmegen), Tobias Müller(University of Würzburg), Pingkalai R. Senthilan(University of Würzburg)
medRxiv
March 30, 2026
Cited by 0


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