Mono and biallelic variants in HCN2 cause severe neurodevelopmental disorders.
Clara Houdayer,A Marie Phillips,Marie Chabbert,Jennifer Bourreau,Reza Maroofian,Henry Houlden,Kay Richards,Nebal Waill Saadi, Eliška Dad'ová,Patrick Van Bogaert, Mailys Rupin,Boris Keren,Perrine Charles,Thomas Smol,Audrey Riquet,Lynn Pais,Anne O'Donnell-Luria,Grace E VanNoy,Allan Bayat,Rikke S Møller,Kern Olofsson,Rami Abou Jamra,Steffen Syrbe, Majed Dasouki,Laurie H Seaver,Jennifer A Sullivan,Vandana Shashi,Fowzan S Alkuraya, Alexis F Poss,J Edward Spence,Rhonda E Schnur,Ian C Forster,Chaseley E Mckenzie,Cas Simons,Min Wang,Penny Snell,Kavitha Kothur,Michael Buckley,Tony Roscioli,Noha Elserafy,Benjamin Dauriat,Vincent Procaccio,Daniel Henrion,Guy Lenaers,Estelle Colin,Nienke E Verbeek,Koen L Van Gassen,Claire Legendre,Dominique Bonneau,Christopher A Reid,Katherine B Howell,Alban Ziegler,Christian Legros medRxiv : the preprint server for health sciences（2024）
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