Journal of Inherited Metabolic Disease

, Volume 22, Issue 8, pp 933–935 | Cite as

Contiguous gene deletion syndrome involving glycerol kinase and Duchenne muscular dystrophy loci

  • M. Asghar
  • N. C. Nevin
  • E. D. Beattie
  • D. McManus
  • G. M. A. Roberts
  • J. A. Phillips
Article
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References

  1. Chelly J, Marlhens F, Dutrillauk B et al (1988) Deletion proximal to DXS68 (L1 probe site) in a boy with Duchenne muscular dystrophy, glycerol kinase deÐciency and adrenal hypoplasia. Hum Genet {78}: 222–227.Google Scholar
  2. Francke U, Harper JF, Darras BT et al (1987) Congenital adrenal hypoplasia, myopathy and glycerol kinase deficiency: molecular evidence for deletions. Am J Hum Genet {40}: 212–227.Google Scholar
  3. McCabe ERB (1995) Disorders of glycerol metabolism. In Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The Metabolic and Molecular Bases of Inherited Disease, 7th edn. New York: McGraw Hill, 1631–1652.Google Scholar

Copyright information

© Kluwer Academic Publishers 1999

Authors and Affiliations

  • M. Asghar
    • 1
  • N. C. Nevin
    • 2
  • E. D. Beattie
    • 2
  • D. McManus
    • 2
  • G. M. A. Roberts
  • J. A. Phillips
    • 1
  1. 1.Department of PaediatricsErne HospitalEnniskillenN. Ireland
  2. 2.Northern Ireland Regional Genetics CentreBelfast City Hospital TrustBelfastN. Ireland

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