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Hereditary variations in monoamine oxidase as a risk factor for Parkinson's disease

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Year: 1994
Type: article
Study design: Observational Study
Source: Movement Disorders
DOI: 10.1002/mds.870090304
Authors: Gokhan S. Hotamisligil, A. Sule Girmen, J. Stephen Fink, Elizabeth Tivol, Christo Shalish, James Trofatter, John Baenziger, Shirley Diamond, Charles Markham, Jack Sullivan, John Growdon, Xandra O. Breakefield
Institutions: Harvard University, Massachusetts General Hospital, Indiana University Indianapolis, Indiana University School of Medicine, Indiana Alcohol Research Center, University of California, Los Angeles
Language: English

Topic: Parkinson's Disease Mechanisms and Treatments
Subfield: Neurology
Field: Medicine
Domain: Health Sciences
SDG: Good health and well-being

Open Access status: closed

Funders: National Institutes of Health, National Institute on Alcohol Abuse and Alcoholism, National Institute of Neurological Disorders and Stroke
Awards: G2108115428, G766033528, BIOCHEMICAL AND GENETIC ANALYSIS OF MONOAMINE OXIDASE
OpenAlex ID: W2020753791
FWCI: 4.005
Cites: 72
Cited by: 67
Related to: 10
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