Further evidence to link CHD family-chromatin remodeler genes and neurodevelopment: de novo variants in CHD5 are associated with intellectual disability, epilepsy and autism

Conference Paper

Full Text

Duke Authors

Cited Authors

  • Lehalle, D; Mizuguchi, T; Nava, C; Matsumoto, N; Cope, H; de Man, S; Friedman, J; Joset, P; Kato, M; Muffels, I; Nakamura, K; Person, RE; Petit, F; Rauch, A; Shashi, V; Smol, T; Steindl, K; Torti, E; Van de Laar, I; Fuchs, S; Depienne, C; Mignot, C

Published Date

  • December 2020

Published In

Volume / Issue

  • 28 / SUPPL 1

Start / End Page

  • 326 - 327

Electronic International Standard Serial Number (EISSN)

  • 1476-5438

International Standard Serial Number (ISSN)

  • 1018-4813