Work

Marked Amine and Amine Metabolite Changes in Norrie Disease Patients with an X‐Chromosomal Deletion Affecting Monoamine Oxidase

Year: 1990

Type: article

Study design: Case Report

Source: Journal of Neurochemistry

DOI: 10.1111/j.1471-4159.1990.tb13307.x

Authors: D. L. Murphy, K. B. Sims, F. Karoum, A. de la Chapelle, R. Norio, E.‐M. Sankila, 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: W2054637867

FWCI: 3.89

Cites: 49

Cited by: 53

Related to: 10