Reply to: "Childhood Onset Chorea Caused by a Recurrent De Novo DRD2 Variant"
Mov Disord
.
2021 Jun;36(6):1473-1474.
doi: 10.1002/mds.28635.
Authors
Marlous C M van der Weijden
1
2
,
Dayana Rodriguez-Contreras
3
,
Kim A Neve
3
4
,
Dineke S Verbeek
1
2
,
Marina A J Tijssen
2
5
Affiliations
1
Department of Genetics, University Medical Center Groningen, Groningen, the Netherlands.
2
Expertise Center Movement Disorders Groningen, University Medical Center Groningen, Groningen, the Netherlands.
3
Department of Behavioral Neuroscience, Oregon Health & Science University, Portland, Oregon, USA.
4
Research Service, VA Portland Health Care System, Portland, Oregon, USA.
5
Department of Neurology, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
PMID:
34145634
DOI:
10.1002/mds.28635
No abstract available
Publication types
Letter
Comment
MeSH terms
Child
Chorea* / genetics
Dystonia*
Gain of Function Mutation
Humans
Phenotype
Receptors, Dopamine D2 / genetics
Substances
DRD2 protein, human
Receptors, Dopamine D2
Grants and funding
I01 BX003279/BX/BLRD VA/United States
R21 NS117713/NS/NINDS NIH HHS/United States