Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy
Titel:
Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy
Auteur:
O’Donnell-Luria, Anne H. Pais, Lynn S. Faundes, Víctor Wood, Jordan C. Sveden, Abigail Luria, Victor Abou Jamra, Rami Accogli, Andrea Amburgey, Kimberly Anderlid, Britt Marie Azzarello-Burri, Silvia Basinger, Alice A. Bianchini, Claudia Bird, Lynne M. Buchert, Rebecca Carre, Wilfrid Ceulemans, Sophia Charles, Perrine Cox, Helen Culliton, Lisa Currò, Aurora Demurger, Florence Dowling, James J. Duban-Bedu, Benedicte Dubourg, Christèle Eiset, Saga Elise Escobar, Luis F. Ferrarini, Alessandra Haack, Tobias B. Hashim, Mona Heide, Solveig Helbig, Katherine L. Helbig, Ingo Heredia, Raul Héron, Delphine Isidor, Bertrand Jonasson, Amy R. Joset, Pascal Keren, Boris Kok, Fernando Kroes, Hester Y. Lavillaureix, Alinoë Lu, Xin Maas, Saskia M. Maegawa, Gustavo H.B. Marcelis, Carlo L.M. Mark, Paul R. Masruha, Marcelo R. McLaughlin, Heather M. McWalter, Kirsty Melchinger, Esther U. Mercimek-Andrews, Saadet Nava, Caroline Pendziwiat, Manuela Person, Richard Ramelli, Gian Paolo Ramos, Luiza L.P. Rauch, Anita Reavey, Caitlin Renieri, Alessandra Rieß, Angelika Sanchez-Valle, Amarilis Sattar, Shifteh Saunders, Carol Schwarz, Niklas Smol, Thomas Srour, Myriam Steindl, Katharina Syrbe, Steffen Taylor, Jenny C. Telegrafi, Aida Thiffault, Isabelle Trauner, Doris A. van der Linden Jr., Helio van Koningsbruggen, Silvana Villard, Laurent Vogel, Ida Vogt, Julie Weber, Yvonne G. Wentzensen, Ingrid M. Widjaja, Elysa Zak, Jaroslav Baxter, Samantha Banka, Siddharth Rodan, Lance H.