Glycogen storage disease type 1b due to a defect of glucose-6-phosphate translocase. | J Inherit Metab Dis;5(4): 227-8, 1982. | MEDLINE

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Glycogen storage disease type 1b due to a defect of glucose-6-phosphate translocase.

Narisawa, K; Otomo, H; Igarashi, Y; Arai, N; Otake, M; Tada, K; Kuzuya, T.

J Inherit Metab Dis ; 5(4): 227-8, 1982.

Article in En | MEDLINE | ID: mdl-6133035

Subject(s)

Glycogen Storage Disease Type I/genetics; Phosphotransferases/deficiency; Antiporters; Glycogen Storage Disease Type I/enzymology; Glycogen Storage Disease Type I/pathology; Humans; Infant; Kinetics; Liver/pathology; Male; Monosaccharide Transport Proteins; Phosphotransferases/genetics; Pyrophosphatases/metabolism

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Collection: 01-internacional Database: MEDLINE Main subject: Phosphotransferases / Glycogen Storage Disease Type I Limits: Humans / Infant / Male Language: En Journal: J Inherit Metab Dis Year: 1982 Document type: Article Country of publication: United States

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Collection: 01-internacional Database: MEDLINE Main subject: Phosphotransferases / Glycogen Storage Disease Type I Limits: Humans / Infant / Male Language: En Journal: J Inherit Metab Dis Year: 1982 Document type: Article Country of publication: United States