Skip to main content
Log in

Urinary and plasma organic acids in dizygotic twin siblings with 3-hydroxy-3-methylglutaric aciduria, studied by gas chromatography and mass spectrometry using fused silica capillary columns

  • Short Communication
  • 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

  • Chalmers, R. A. and Lawson, A. M.Organic Acids in Man, Chapman and Hall, London, 1982

    Google Scholar 

  • Chalmers, R. A. and Watts, R. W. E. The quantitative extraction and gas liquid chromatographic determination of organic acids in urine.Analyst 97 (1972) 958–963

    PubMed  Google Scholar 

  • Robinson, B. H., Oei, J., Sherwood, W. G., Slyper, A. H., Heininger, J. and Mamer, O. A. Hydroxymethylglutaryl CoA lyase deficiency: Features resembling Reye syndrome.Neurology 30 (1980) 714–718

    PubMed  Google Scholar 

  • Norman, E. J., Denton, M. D. and Berry, H. K. Gaschromatographic mass spectrometric detection of 3-hydroxy-3-methylglutaryl-CoA lyase deficiency in first cousinsClin. Chem. 28 (1982) 137–140

    PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Tracey, B.M., Stacey, T.E. & Chalmers, R.A. Urinary and plasma organic acids in dizygotic twin siblings with 3-hydroxy-3-methylglutaric aciduria, studied by gas chromatography and mass spectrometry using fused silica capillary columns. J Inherit Metab Dis 6 (Suppl 2), 125–126 (1983). https://doi.org/10.1007/BF01810359

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01810359

Keywords

Navigation