CUL3-related neurodevelopmental disorder: Clinical phenotype of 20 new individuals and identification of a potential phenotype-associated episignature
Titel:
CUL3-related neurodevelopmental disorder: Clinical phenotype of 20 new individuals and identification of a potential phenotype-associated episignature
Auteur:
van der Laan, Liselot Silva, Ananília Kleinendorst, Lotte Rooney, Kathleen Haghshenas, Sadegheh Lauffer, Peter Alanay, Yasemin Bhai, Pratibha Brusco, Alfredo de Munnik, Sonja de Vries, Bert B.A. Vega, Angelica Delgado Engelen, Marc Herkert, Johanna C. Hochstenbach, Ron Hopman, Saskia Kant, Sarina G. Kira, Ryutaro Kato, Mitsuhiro Keren, Boris Kroes, Hester Y. Levy, Michael A. Lock-Hock, Ngu Maas, Saskia M. Mancini, Grazia M.S. Marcelis, Carlo Matsumoto, Naomichi Mizuguchi, Takeshi Mussa, Alessandro Mignot, Cyril Närhi, Anu Nordgren, Ann Pfundt, Rolph Polstra, Abeltje M. Trajkova, Slavica van Bever, Yolande José van den Boogaard, Marie van der Smagt, Jasper J. Barakat, Tahsin Stefan Alders, Mariëlle Mannens, Marcel M.A.M. Sadikovic, Bekim van Haelst, Mieke M. Henneman, Peter