Revising rapid‐onset dystonia–parkinsonism: Broadening indications for ATP1A3 testing-Reference-Cited by-同舟云学术

Revising rapid‐onset dystonia–parkinsonism: Broadening indications for ATP1A3 testing

Published:2019-07-30 Issue:10 Volume:34 Page:1528-1536
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord

Author:

Haq Ihtsham U.¹^ORCID,Snively Beverly M.²,Sweadner Kathleen J.³,Suerken Cynthia K.²,Cook Jared F.¹,Ozelius Laurie J.⁴,Miller Charlotte¹,McCall William V.⁵,Whitlow Christopher T.⁶,Brashear Allison¹

Affiliation:

1. Department of Neurology Wake Forest School of Medicine Winston‐Salem North Carolina USA

2. Department of Biostatistical Sciences Wake Forest School of Medicine Winston‐Salem North Carolina USA

3. Department of Neurosurgery Massachusetts General Hospital Boston Massachusetts USA

4. Department of Neurology Massachusetts General Hospital Boston Massachusetts USA

5. Department of Psychiatry and Health Behavior Medical College of Georgia August University Augusta Georgia USA

6. Department of Radiology, Section of Neuroradiology Wake Forest School of Medicine Winston‐Salem North Carolina USA

Funder

National Institute of Neurological Disorders and Stroke

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mds.27801

Reference35 articles.

1. Rapid-onset dystonia-parkinsonism

2. The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene

3. Rapid-onset dystonia-parkinsonism: A clinical and genetic analysis of a new kindred

4. Mutations in the Na+/K+-ATPase α3 Gene ATP1A3 Are Associated with Rapid-Onset Dystonia Parkinsonism

5. Distribution of Na/K-ATPase alpha 3 isoform, a sodium-potassium P-type pump associated with rapid-onset of dystonia parkinsonism (RDP) in the adult mouse brain

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