FRMPD4, a causal gene for intellectual disability and epilepsy, is associated with X-linked non-syndromic hearing loss
Daniel Liedtke, K Rak, Katrina M. Schrode, Philip Hehlert, Niloofar Chamanrou, Daniel Bengl, Radoslaw Katana, Soganad Heydaran, Julia Doll, Mei Han, Indrajit Nanda, Pingkalai R. Senthilan, Lukas Juergens, Linda Bieniussa, Johannes Voelker, , Barbara Vona
The paper identifies FRMPD4 as a causal gene for X-linked non-syndromic hearing loss through genetic analysis and cross-species functional studies.
medRxiv · Mar 30, 2026 · PreprintGenetic & Genomic Medicine