| Literature DB >> 30935829 |
Christine Klein1, Hauke Baumann1, Luisa Olschewski1, Henrike Hanssen2, Alexander Münchau1, Andreas Ferbert3, Norbert Brüggemann2, Katja Lohmann4.
Abstract
Entities:
Keywords: Consanguinity; De-novo mutation; Dyscalculia; Gene expression; Generalized dystonia; KMT2B
Mesh:
Substances:
Year: 2019 PMID: 30935829 DOI: 10.1016/j.parkreldis.2019.03.018
Source DB: PubMed Journal: Parkinsonism Relat Disord ISSN: 1353-8020 Impact factor: 4.891