Glutathionuria: inborn error of metabolism due to tissue deficiency of gamma-glutamyl transpeptidase.

Biochemical and biophysical research communications ·Vol. 65 ·No. 1 ·1975-07-08 ·Pages 68-74

Schulman JD, Goodman SI, Mace JW, Patrick AD, Tietze F, Butler EJ

Abstract

暂无摘要

MeSH Terms

Adult Amino Acid Metabolism, Inborn Errors/enzymology Amino Acids/blood,urine Cells, Cultured Fibroblasts/enzymology Glutathione/blood,metabolism,urine Humans Intellectual Disability/enzymology Male Skin/enzymology gamma-Glutamyltransferase/metabolism

Chemicals

Amino Acids gamma-Glutamyltransferase Glutathione

Authors & Affiliations

6 authors, click to expand affiliations / ORCID

Schulman J D

Goodman S I

Mace J W

Patrick A D

Tietze F

Butler E J

Article Info

Journal

Biochemical and biophysical research communications

Abbr.

Biochem Biophys Res Commun

ISSN

0006-291X

DOI

10.1016/s0006-291x(75)80062-3

Published

1975-07-08

Pages

68-74

Language

English

Region

United States

NLM ID

0372516

Subset

External Links

PubMed source DOI: 10.1016/s0006-291x(75)80062-3 View journal details

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Glutathionuria: inborn error of metabolism due to tissue deficiency of gamma-glutamyl transpeptidase.

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