Work

Dystonia in ATP2B3‐associated X‐linked spinocerebellar ataxia

Year: 2016

Type: article

Abstract: Additional Supporting Information may be found in the online version of this article. Supporting Information Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.

Source: Movement Disorders

DOI: 10.1002/mds.26800

Authors: Timothy Feyma, Keri Ramsey, Matthew J. Huentelman, David W. Craig, Sergio Padilla‐Lopez, Vinodh Narayanan, Michael C. Kruer

Institutions: Gillette Children's Specialty Healthcare, Translational Genomics Research Institute, Arizona State University, Phoenix Children's Hospital, University of Arizona College of Medicine- Phoenix

Language: English

Topic: Genetic Neurodegenerative Diseases

Subfield: Cellular and Molecular Neuroscience

Field: Neuroscience

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: green

Funders: Doris Duke Charitable Foundation, National Institute of Neurological Disorders and Stroke

Awards: G4899527354, Molecular mechanisms of mitochondrial dysfunction in ATP13A2-associated neurodege

OpenAlex ID: W2525682839

FWCI: 1.226

Cites: 3

Cited by: 23

Related to: 10