Reply to: “Childhood Onset Chorea Caused by a Recurrent De Novo DRD2 Variant”-Reference-Cited by-同舟云学术

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Reply to: “Childhood Onset Chorea Caused by a Recurrent De Novo DRD2 Variant”

Published:2021-06 Issue:6 Volume:36 Page:1473-1474
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord

Author:

Weijden Marlous C.M.¹²^ORCID,Rodriguez‐Contreras Dayana³,Neve Kim A.³⁴^ORCID,Verbeek Dineke S.¹²^ORCID,Tijssen Marina A.J.²⁵^ORCID

Affiliation:

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

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mds.28635

Reference2 articles.

1. A Gain‐of‐Function Variant in Dopamine D2 Receptor and Progressive Chorea and Dystonia Phenotype

2. Developmental origins of brain disorders: roles for dopamine

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Comparison of the function of two novel human dopamine D2 receptor variants identifies a likely mechanism for their pathogenicity;Biochemical Pharmacology;2024-04

2. Gait Abnormalities and Aberrant D2 Receptor Expression and Signaling in Mice Carrying the Human Pathogenic MutationDRD2^I212F;Molecular Pharmacology;2022-12-01

3. Gait Abnormalities and Aberrant D2 Receptor Expression and Signaling in a Mouse Model of the Human Pathogenic Mutation DRD2^I212F;2022-06-11

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