Work

PINK1 ‐Associated Juvenile‐Onset Parkinsonism: Marked Phenotypic Variability and Limited Genotype–Phenotype Correlation

Year: 2026

Type: article

Source: Movement Disorders

DOI: 10.1002/mds.70502

Authors: Reza Maroofian, Ross Leng, Shilpan G. Patel, Hina Ojha, Heba Hosny, Maha Zaki, Miratul M.K. Muqit, Henry Houlden

Institutions: UK Dementia Research Institute, UCL Queen Square Institute of Neurology, University College London, University of Dundee, MRC Protein Phosphorylation and Ubiquitylation Unit, The National Institute of Neuromotor System, National Research Centre, University of Edinburgh

Language: English

Topic: Parkinson's Disease Mechanisms and Treatments

Subfield: Clinical Neurology

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: hybrid

Estimated APC paid: $4,480

Funders: Michael J. Fox Foundation for Parkinson's Research, National Ataxia Foundation, Wellcome Trust, Target ALS, Parkinson's Foundation, National Brain Appeal, National Institute for Health and Care Research, Parkinson's UK, Ataxia UK, University College London, European Commission, Rosetrees Trust, UK Dementia Research Institute, National Institutes of Health, HORIZON EUROPE Framework Programme, Medical Research Council, NIHR Sheffield Biomedical Research Centre

Award: Understanding non-coding genomic variation in neurological disorders

OpenAlex ID: W7204858824

FWCI:

Cites: 5

Cited by:

Related to: 10