Reply to "Truncating VPS16 Mutations are Rare in Early-Onset Dystonia"
Ann Neurol
.
2021 Mar;89(3):626.
doi: 10.1002/ana.25988.
Epub 2020 Dec 22.
Authors
Michael Zech
1
2
,
Dora Steel
3
4
,
Manju A Kurian
3
4
,
Juliane Winkelmann
1
2
5
6
Affiliations
1
Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany.
2
Institute of Human Genetics, Technical University of Munich, Munich, Germany.
3
Department of Developmental Neurosciences, UCL Great Ormond Street Institute of Child Health, London, UK.
4
Department of Neurology, Great Ormond Street Hospital, London, UK.
5
Lehrstuhl für Neurogenetik, Technische Universität München, Munich, Germany.
6
Munich Cluster for Systems Neurology, Munich, Germany.
PMID:
33305837
DOI:
10.1002/ana.25988
No abstract available
Publication types
Letter
Comment
MeSH terms
Dystonia* / genetics
Dystonic Disorders* / genetics
Humans
Lysosomes
Mutation / genetics
Vesicular Transport Proteins / genetics
Substances
VPS16 protein, human
VPS41 protein, human
Vesicular Transport Proteins
Grants and funding
RP-2016-07-019/DH_/Department of Health/United Kingdom