A de novo GRIA3 variant with complex hyperkinetic movement disorder in a girl with developmental delay and self-limited epilepsy
Parkinsonism & related disorders.
2023 Jun ;
111 () :
105437.
[epub] 20230505
Language English Country England, Great Britain Media print-electronic
Document type Letter, Research Support, Non-U.S. Gov't
Persistent link
https://www.medvik.cz/link/pmid37163803
PubMed
37163803
DOI
10.1016/j.parkreldis.2023.105437
PII: S1353-8020(23)00160-8
Knihovny.cz E-resources
- MeSH
- Epilepsy * genetics MeSH
- Attention Deficit Disorder with Hyperactivity * MeSH
- Hyperkinesis genetics MeSH
- Humans MeSH
- Check Tag
- Humans MeSH
- Female MeSH
- Publication type
- Letter MeSH
- Research Support, Non-U.S. Gov't MeSH
References provided by Crossref.org
