Etiological involvement of KCND1 variants in an X-linked neurodevelopmental disorder with variable expressivity
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Published:2024-06
Issue:6
Volume:111
Page:1206-1221
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ISSN:0002-9297
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Container-title:The American Journal of Human Genetics
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language:en
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Short-container-title:The American Journal of Human Genetics
Author:
Kalm Tassja, Schob Claudia, Völler Hanna, Gardeitchik Thatjana, Gilissen Christian, Pfundt Rolph, Klöckner Chiara, Platzer Konrad, Klabunde-Cherwon Annick, Ries Markus, Syrbe Steffen, Beccaria Francesca, Madia Francesca, Scala Marcello, Zara Federico, Hofstede Floris, Simon Marleen E.H., van Jaarsveld Richard H., Oegema Renske, van Gassen Koen L.I., Holwerda Sjoerd J.B., Barakat Tahsin Stefan, Bouman Arjan, van Slegtenhorst Marjon, Álvarez Sara, Fernández-Jaén Alberto, Porta Javier, Accogli Andrea, Mancardi Margherita Maria, Striano Pasquale, Iacomino Michele, Chae Jong-Hee, Jang SeSong, Kim Soo Y., Chitayat David, Mercimek-Andrews Saadet, Depienne Christel, Kampmeier Antje, Kuechler Alma, Surowy Harald, Bertini Enrico Silvio, Radio Francesca Clementina, Mancini Cecilia, Pizzi Simone, Tartaglia Marco, Gauthier Lucas, Genevieve David, Tharreau Mylène, Azoulay Noy, Zaks-Hoffer Gal, Gilad Nesia K., Orenstein Naama, Bernard Geneviève, Thiffault Isabelle, Denecke Jonas, Herget Theresia, Kortüm Fanny, Kubisch Christian, Bähring Robert, Kindler StefanORCID
Funder
Ministero della Salute Quebec Health Research Fund Italian Association of Mechanical Technology German Research Foundation Nederlandse Organisatie voor Wetenschappelijk Onderzoek Erasmus Medisch Centrum ZonMw Erasmus MC Vriendenfonds Canadian Institutes of Health Research
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