Etiological involvement of KCND1 variants in an X-linked neurodevelopmental disorder with variable expressivity - 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; et al. (The American journal of human genetics, 2024)
Gesehen am 27.05.2024