Missense and truncating variants in CHD5 in a dominant neurodevelopmental disorder with intellectual disability, behavioral disturbances, and epilepsy

2021 . Parenti, Ilaria | Lehalle, Daphné | Nava, Caroline | Torti, Erin | Leitão, Elsa | Person, Richard | Mizuguchi, Takeshi | Matsumoto, Naomichi | Kato, Mitsuhiro | Nakamura, Kazuyuki | de Man, Stella | Cope, Heidi | Shashi, Vandana | Friedman, Jennifer | Joset, Pascal | Steindl, Katharina | Rauch, Anita | Muffels, Irena | van Hasselt, Peter M | petit, florence | Smol, Thomas | Le Guyader, Gwenaël | Bilan, Frédéric | Sorlin, Arthur | Vitobello, Antonio | PHILIPPE, Christophe | van de Laar, Ingrid | van Slegtenhorst, Marjon A. | Campeau, Philippe | Au, Ping Yee | Nakashima, Mitsuko | Saitsu, Hirotomo | Yamamoto, Tatsuya | Nomura, Yumiko | Louie, Raymond | Lyons, Michael | Dobson, Amy | Plomp, Astrid S. | Motazacker, M. Mahdi | Kaiser, Frank J. | Timberlake, Andrew | Fuchs, Sabine | Depienne, Christel | Mignot, Cyril