Treffer: Mechanism of KMT5B haploinsufficiency in neurodevelopment in humans and mice
Title:
Mechanism of KMT5B haploinsufficiency in neurodevelopment in humans and mice
Authors:
Sheppard, Sarah E, Bryant, Laura, Wickramasekara, Rochelle N, Vaccaro, Courtney, Robertson, Brynn, Hallgren, Jodi, Hulen, Jason, Watson, Cynthia J, Faundes, Victor, Duffourd, Yannis, Lee, Pearl, Simon, M Celeste, de la Cruz, Xavier, Padilla, Natália, Flores-Mendez, Marco, Akizu, Naiara, Smiler, Jacqueline, Da Silva, Renata Pellegrino, Li, Dong, March, Michael, Diaz-Rosado, Abdias, de Barcelos, Isabella Peixoto, Choa, Zhao Xiang, Lim, Chin Yan, Dubourg, Christèle, Journel, Hubert, Demurger, Florence, Mulhern, Maureen, Akman, Cigdem, Lippa, Natalie, Joset, Pascal, Steindl, Katharina, Rauch, Anita, et al
Contributors:
University of Zurich
Publisher Information:
American Association for the Advancement of Science, 2023.
Publication Year:
2023
Subject Terms:
1000 Multidisciplinary, Methyltransferases / genetics, 10039 Institute of Medical Genetics, Knockout, 610 Medicine & health, Haploinsufficiency, Methyltransferases, Mice, Phenotype, Megalencephaly, 10036 Medical Clinic, U9 Adaptive Brain Circuits in Development and Learning (AdaBD), Neurodevelopmental Disorders* / genetics, 570 Life sciences, biology, Animals, Humans
Document Type:
Other literature type<br />Article
File Description:
sciadv.ade1463.pdf - application/pdf
DOI:
10.5167/uzh-232351
Rights:
CC BY NC
Accession Number:
edsair.doi.dedup.....9be16f00ccd7a9581baf8dce19ef91a2
Database:
OpenAIRE