Severe paroxysmal dyskinesias without epilepsy in a RHOBTB2 mutation carrier
Language English Country England, Great Britain Media print-electronic
Document type Case Reports, Letter, Research Support, Non-U.S. Gov't
PubMed
32653842
DOI
10.1016/j.parkreldis.2020.06.028
PII: S1353-8020(20)30205-4
Knihovny.cz E-resources
- MeSH
- Dyskinesias diagnosis genetics MeSH
- Epilepsy diagnosis genetics MeSH
- Humans MeSH
- Mutation genetics MeSH
- Tumor Suppressor Proteins genetics MeSH
- GTP-Binding Proteins genetics MeSH
- Check Tag
- Humans MeSH
- Female MeSH
- Publication type
- Letter MeSH
- Case Reports MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Tumor Suppressor Proteins MeSH
- GTP-Binding Proteins MeSH
- RHOBTB2 protein, human MeSH Browser
2nd Pediatric Clinic Slovak Medical University Banská Bystrica Slovakia
Department of Clinical Genetics Faculty Hospital Trenčín Trenčín Slovakia
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