Neurodevelopmental Gene-Related Dystonia-Parkinsonism with Onset in Adults: A Case with NAA15 Variant

Mov Disord. 2022 Sep;37(9):1955-1957. doi: 10.1002/mds.29125. Epub 2022 Jun 22.

Authors

Igor Straka¹, Jana Švantnerová¹, Michal Minár¹, Simona Stanková¹, Michael Zech^{2

3}

Affiliations

¹ Second Department of Neurology, Faculty of Medicine, Comenius University, University Hospital Bratislava, Bratislava, Slovakia.
² Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany.
³ Institute of Human Genetics, School of Medicine, Technical University of Munich, Munich, Germany.

PMID: 35730864
DOI: 10.1002/mds.29125

No abstract available

Keywords: NAA15; dystonia; neurodevelopmental disorder; parkinsonism.

Publication types

Letter
Research Support, Non-U.S. Gov't

MeSH terms

Adult
Dystonia* / complications
Dystonia* / genetics
Dystonic Disorders* / complications
Dystonic Disorders* / genetics
Humans
N-Terminal Acetyltransferase A
N-Terminal Acetyltransferase E
Parkinsonian Disorders* / complications
Parkinsonian Disorders* / genetics

Substances

NAA15 protein, human
N-Terminal Acetyltransferase A
N-Terminal Acetyltransferase E