Log in

Renal tubular dysfunction in multiple acyl-CoA dehydrogenase deficiency

  • Published:
Journal of Inherited Metabolic Disease

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

Access this article

Subscribe and save

Springer+ Basic
EUR 32.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or Ebook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

Price includes VAT (Germany)

Instant access to the full article PDF.

REFERENCES

  • Falik-Borenstein ZC, Jordan SC, Saudubray JM, et al (1992) Renal tubular acidosis in carnitine palmitoyltransferase type I deficiency. N Engl J Med 327: 24–27.

    Google Scholar 

  • Frerman FE, Goodman SI (1995) Nuclear-encoded defects of the mitochondrial respiratory chain, including glutaric aciduria type II. In Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The Metabolic and Molecular Bases of Inherited Disease, 7th edn. New York: McGraw-Hill, 1611–1629.

    Google Scholar 

  • Manning NJ, Olpin SE, Pollitt R, Webley J (1990) A comparison of [9,10-3H]palmitic and [9,10-3H]-myristic acids for the detection of defects of fatty acid oxidation in intact cultured fibroblasts. J Inher Metab Dis 13: 58–68.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Morris, A.A.M., Olpin, S.E., Van't Hoff, W.G. et al. Renal tubular dysfunction in multiple acyl-CoA dehydrogenase deficiency. J Inherit Metab Dis 20, 604–605 (1997). https://doi.org/10.1023/A:1005371428912

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1005371428912

Navigation