Hypoglycinaemia and psychomotor delay in a child with xeroderma pigmentosum

Journal of Inherited Metabolic Disease

Volumn 22, Issue 8, 1999, Pages 915-924

  Quackenbush, E J ^a,b   Kraemer, K H ^c   Gahl, W A ^d   Schirch, V ^e   Whiteman, D A H ^f   Levine, K ^a   Levy, H L ^a  

^a BOSTON CHILDREN S HOSPITAL   (United States)

^b CENTER FOR BLOOD RESEARCH   (United States)

^c NATIONAL CANCER INSTITUTE   (United States)

^d EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH AND HUMAN DEVELOPMENT   (United States)

^e VIRGINIA COMMONWEALTH UNIVERSITY   (United States)

^f MAINE MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GLYCINE; SERINE;

ARTICLE; AUTISM; CASE REPORT; CLINICAL FEATURE; COGNITIVE DEFECT; HUMAN; HYPERACTIVITY; MALE; MUSCLE HYPOTONIA; MUTISM; ORAL DRUG ADMINISTRATION; PRESCHOOL CHILD; PSYCHOMOTOR RETARDATION; XERODERMA PIGMENTOSUM;

AMINO ACIDS; CHILD; GLYCINE HYDROXYMETHYLTRANSFERASE; HUMANS; HYPOGLYCEMIA; LIVER; MALE; PSYCHOMOTOR PERFORMANCE; XERODERMA PIGMENTOSUM;

EID: 0032738223     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1005691424004     Document Type: Article

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