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Glycogen phosphorylase b kinase deficiency in three siblings

  • Case Report
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Journal of Inherited Metabolic Disease

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Reference

  • Schimke, R. N., Zakheim, M. D., Corder, R. C. and Hug, M. D. Glycogen storage disease type IX: Benign glycogenosis of liver and hepatic phosphorylase kinase deficiency.J. Pediatr. 83 (1973) 1031–1034

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Authors and Affiliations

  1. University Sub-Department of Medical Genetics, UK

    R. G. F. Gray

  2. Centre for Human Genetics, 117 Manchester Road, S10 5DN, Sheffield, UK

    D. Kumar

  3. Institute of Child Health, 30 Guilford Street, WC1N 1EH, London, UK

    A. E. Whitfield

Authors
  1. R. G. F. Gray
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  2. D. Kumar
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  3. A. E. Whitfield
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Gray, R.G.F., Kumar, D. & Whitfield, A.E. Glycogen phosphorylase b kinase deficiency in three siblings. J Inherit Metab Dis 6, 107 (1983). https://doi.org/10.1007/BF01800737

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  • DOI: https://doi.org/10.1007/BF01800737

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