Skip to main content
Log in

Generalized glutathione synthetase deficiency and pregnancy

  • Published:
Journal of Inherited Metabolic Disease

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

References

  • Dahl N, Pigg M, Risto. E, et al (1997) Missense mutations in human glutathione synthetase gene result in severe metabolic acidosis, 5-oxoprolinuria, haemolytic anaemia and neurological dysfunction. Hum Mol Genet 6(7): 1147-1152.

    Google Scholar 

  • Larsson A, Anderson M (1999) Glutathione synthetase deficiency and other disorders of the γ-glutamyl cycle. In Scriver CF, Beaudet AL, Sly WS, Valle D, eds. The Metabolic and Molecular Bases of Inherited Disease, 8th edn. New York: McGraw-Hill, in press.

    Google Scholar 

  • Larsson A, Zetterstöm R, Hagenfeldt L, Andersson R, Dreborg S, Hörnell H (1974) Pyroglutamic aciduria (5-oxoprolinuria), an inborn error in glutathione metabolism. Pediatr Res 8: 852-856.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Ristoff, E., Augustson, C. & Larsson, A. Generalized glutathione synthetase deficiency and pregnancy. J Inherit Metab Dis 22, 758–759 (1999). https://doi.org/10.1023/A:1005564705898

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1005564705898

Keywords

Navigation