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Hypoglycinaemia and psychomotor delay in a child with xeroderma pigmentosum

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Year: 1999
Type: article
Study design: Case Report
Source: Journal of Inherited Metabolic Disease
DOI: 10.1023/a:1005691424004
Authors: E. J. Quackenbush, K. H. Kraemer, W. A. Gahl, V. Schirch, D. A. H. Whiteman, K. Levine, H. L. Levy
Institutions: Boston Children's Hospital, National Institutes of Health, National Cancer Institute, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Virginia Commonwealth University, Maine Medical Center
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 Cancer Institute
Award: DNA Repair in Human Cancer-Prone Genetic Diseases
OpenAlex ID: W1506689393
FWCI:
Cites: 27
Cited by: 9
Related to: 10
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