KCNB1 mutations are causing a neurodevelopmental disorder including epilepsy and autism
Year: 2017
Type: article
Source: Epilepsia
Authors: Rikke S. Møller, Carolien G. F. de Kovel, Steffan Syrbe, Bitten Schönewolf‐Greulich, Mette Rokkjær, Dea Svaneby, Line H.G. Larsen, Eva H. Brilstra, Nienke E. Verbeek, Bronwyn Kerr, Holly Dubbs, Allan Bayat, Soaham Desai, S. Naidu, Shalini Srivastava, H. Caglayan, Uluç Yiş, Carol J. Saunders, M. Rook, S. Plugge, V Jayaraman, Rukkumani Rajagopalan, Ethan M. Goldberg, Eric D. Marsh, Sudha Kilaru Kessler, Christina Bergqvist, Laura K. Conlin, Bryan L. Krock, Isabelle Thiffault, Manuela Pendziwiat, Ingo Helbig, Tilman Polster, Ingo Borggräfe, Johannes R. Lemke, M.-J. van den Boogaardt, Elena Gardella, B. P. C. Köleman
Language: English
Subfield: Psychiatry and Mental health
Field: Medicine
Domain: Health Sciences
Open Access status: closed
OpenAlex ID: W2884606090