Work

Compound heterozygosity in four asymptomatic siblings with medium‐chain acyl‐CoA dehydrogenase deficiency

Year: 2001

Type: article

Source: Journal of Inherited Metabolic Disease

DOI: 10.1023/a:1010533408635

Authors: S. Albers, H. L. Levy, M. Irons, A. W. Strauss, D. Marsden

Institutions: Boston Children's Hospital, Harvard University, Vanderbilt University, University of Massachusetts Chan Medical School

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: U.S. Public Health Service, National Human Genome Research Institute

Awards: G2828648028, Expanded Newborn Screening for Metabolic Disorders, G8915928492

OpenAlex ID: W1498144141

FWCI: 0.186

Cites: 3

Cited by: 7

Related to: 10