Clinical and biochemical observations on a child with a deficiency of 3-hydroxy-3-methylglutaryl coenzyme A lyase. | J Inherit Metab Dis;3(3): 89-90, 1980. | MEDLINE

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Clinical and biochemical observations on a child with a deficiency of 3-hydroxy-3-methylglutaryl coenzyme A lyase.

Ketel, A; Ket, J L; Schutgens, R B; Duran, M; Wadman, S K.

J Inherit Metab Dis ; 3(3): 89-90, 1980.

Article in En | MEDLINE | ID: mdl-6158624

Subject(s)

Oxo-Acid-Lyases/deficiency; Acyl Coenzyme A/deficiency; Acyl Coenzyme A/urine; Amino Acid Metabolism, Inborn Errors/diet therapy; Amino Acid Metabolism, Inborn Errors/therapy; Amino Acid Metabolism, Inborn Errors/urine; Carboxylic Acids/urine; Glucose/administration & dosage; Humans; Infant; Meglutol/analogs & derivatives; Meglutol/deficiency; Meglutol/urine; Oxo-Acid-Lyases/urine

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Collection: 01-internacional Database: MEDLINE Main subject: Oxo-Acid-Lyases Limits: Humans / Infant Language: En Journal: J Inherit Metab Dis Year: 1980 Document type: Article Country of publication: United States

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Collection: 01-internacional Database: MEDLINE Main subject: Oxo-Acid-Lyases Limits: Humans / Infant Language: En Journal: J Inherit Metab Dis Year: 1980 Document type: Article Country of publication: United States