Work

Ornithine carbamoyltransferase deficiency: Unusual clinical findings and novel mutation

Year: 1999

Type: article

Source: Journal of Inherited Metabolic Disease

DOI: 10.1023/a:1005502718790

Authors: V. E. Shih, A. P. Safran, A. H. Ropper, M. Tuchman

Institutions: Harvard University, Massachusetts General Hospital, St. Elizabeth's Medical Center, University of Minnesota

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

Funder: National Institute of Neurological Disorders and Stroke

Awards: NEW AMINO ACID DISORDERS IN CEREBRAL DISEASE, G714539263

OpenAlex ID: W199849721

FWCI:

Cites: 3

Cited by: 2

Related to: 10