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Trisomy X syndrome with dystonia and a pathogenic SATB1 variant
J. Necpál, M. Zech, J. Winkelmann, R. Jech
Neurological sciences.
2021 ;
42 (9) :
3883-3884.
[pub] 20210524
Language English Country Italy
Document type Letter
Persistent link
https://www.medvik.cz/link/bmc21025054
- MeSH
- Sex Chromosome Aberrations MeSH
- Dystonia * genetics MeSH
- Humans MeSH
- Chromosomes, Human, X MeSH
- Sex Chromosome Disorders of Sex Development * MeSH
- Trisomy genetics MeSH
- Matrix Attachment Region Binding Proteins * genetics MeSH
- Check Tag
- Humans MeSH
- Publication type
- Letter MeSH
Department of Neurology Zvolen Hospital Zvolen Slovakia
Institute of Human Genetics Technical University of Munich Munich Germany
Institute of Neurogenomics Helmholtz Zentrum München Munich Germany
Lehrstuhl für Neurogenetik Technische Universität München Munich Germany
References provided by Crossref.org
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