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Plasma amine oxidase activities in Norrie disease patients with an X-chromosomal deletion affecting monoamine oxidase

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Year: 1991
Type: article
Study design: Observational Study
Source: Journal of Neural Transmission
DOI: 10.1007/bf01244447
Authors: D. L. Murphy, K. B. Sims, F. Karoum, N. A. Garrick, A. Chapelle, E. M. Sankila, R. Norio, X. O. Breakefield
Institutions: National Institute of Mental Health, Massachusetts General Hospital, Eunice Kennedy Shriver Center, St. Elizabeths Hospital, University of Helsinki, Väestöliitto, Harvard University
Language: English

Topic: Metabolism and Genetic Disorders
Subfield: Clinical Biochemistry
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: closed

Funders: National Institutes of Health, National Institute of Neurological Disorders and Stroke, Eunice Kennedy Shriver National Institute of Child Health and Human Development
Awards: G2588433142, MOLECULAR GENETIC STUDY OF CHROMOSOME 21 GENE EXPRESSION, G3926132417, BIOCHEMICAL AND GENETIC ANALYSIS OF MONOAMINE OXIDASE
OpenAlex ID: W2022318617
FWCI: 1.636
Cites: 61
Cited by: 29
Related to: 10
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