Work

Novel mutations in the gene encoding very long‐chain acyl‐CoA dehydrogenase identified in patients with partial carnitine palmitoyltransferase ii deficiency

Year: 2012

Type: article

Study design: Observational Study

Source: Muscle & Nerve

DOI: 10.1002/mus.23498

Authors: Paul J. Isackson, Kristin A. Sutton, Karl Y. Hostetler, Georgirene D. Vladutiu

Institutions: University at Buffalo, State University of New York, Hauptman-Woodward Medical Research Institute, University of California San Diego, Veterans Medical Research Foundation of San Diego

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 Arthritis and Musculoskeletal and Skin Diseases

Award: Role of Narexin in Neuromuscular Disease

OpenAlex ID: W2077596821

FWCI: 1.232

Cites: 27

Cited by: 13

Related to: 10