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Glycerol kinase deficiency and adrenal hypoplasia congenita

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Journal of Inherited Metabolic Disease

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REFERENCES

  • Muscatelli F, Strom TF, Walker AP, et al (1994) Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism. Nature 372: 672–676.

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  • Newsholme EA, Robinson J, Taylor KA (1967) Radiochemical enzymatic activity assay for glycerol kinase and hexokinase. Biochim Biophys Acta 132: 338–346.

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  • Walker AP, Muscatelli F, Monaco AP (1993) Isolation of the human Xp21 glycerol kinase gene by positional cloning. Hum Mol Genet 2: 107–114.

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Authors and Affiliations

  1. School of Biochemistry and Molecular Genetics, University of NSW, Sydney, New South Wales, Australia

    R. A. Clarke, W. J. O'Sullivan, L. G. Svirklys & A. G. Mackinlay

  2. Prince of Wales Hospital, Kensington, New South Wales, Australia

    N. Howard

Authors
  1. R. A. Clarke
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  2. N. Howard
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  3. W. J. O'Sullivan
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  4. L. G. Svirklys
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  5. A. G. Mackinlay
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Clarke, R.A., Howard, N., O'Sullivan, W.J. et al. Glycerol kinase deficiency and adrenal hypoplasia congenita. J Inherit Metab Dis 20, 609 (1997). https://doi.org/10.1023/A:1005327713890

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  • DOI: https://doi.org/10.1023/A:1005327713890

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