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Publication
Property Value
Working Groups RG Vona
Subproject A03
Open Access Open Access  Yes
Publication Type Preprint
Peer Reviewed No
DOI DOI  10.64898/2026.03.27.26349271
Publication Year 2026
Title FRMPD4, a causal gene for intellectual disability and epilepsy, is associated with X-linked non-syndromic hearing loss
Journal medRxiv
eISSN 3067-2007
URL  https://doi.org/10.64898/2026.03.27.26349271
Journal Abbreviation medRxiv
Extra Not yet finally published in a peer-reviewed journal
Authors Liedtke D, Rak K, Schrode KM, Hehlert P, Chamanrou N, Bengl D, Katana R, Heydaran S, Doll J, Han M, Nanda I, Senthilan PR, Jürgens L, Bieniussa L, Voelker J, Neuner C, Hofrichter MA, Schröder J, Schellens RT, de Vrieze E, van Wijk E, Zechner U, Herms S, Hoffmann P, Müller T, Dittrich M, Bartsch O, Krawitz PM, Klopocki E, Shehata-Dieler W, Maroofian R, Wang T, Worley PF, Göpfert MC, Galehdari H, Lauer AM, Haaf T, Vona B
First Author Liedtke D
Last Author Vona B

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 1393 Published Data Registry entry (MBExC)