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Mutation spectrum in patients with fructose-1,6-bisphosphatase deficiency

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Journal of Inherited Metabolic Disease

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REFERENCES

  • Herzog B,Wendel U,Morris AAM,Eschrich K (1999) Novel mutations in patients with fructose-1,6-bisphosphatase deficiency. J Inherit Metab Dis 22: 132–138.

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  • Kikawa Y,Inuzuka M,Jin BY, et al (1997) Identification of genetic mutations in Japanese patients with fructose-1,6-bisphosphatase deficiency. Am J Hum Genet 61: 852–861.

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Authors and Affiliations

  1. Institute of Biochemistry, University of Leipzig, Germany

    B. Herzog & K. Eschrich

  2. Department of Child Health, Royal Victoria Infirmary, University of Newcastle upon Tyne, UK

    A. A. M. Morris

  3. Division of Medical Genetics, Department of Pediatrics, Emory University School of Medicine, Atlanta, Georgia, USA

    C. Saunders

Authors
  1. B. Herzog
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  2. A. A. M. Morris
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  3. C. Saunders
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  4. K. Eschrich
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Herzog, B., Morris, A.A.M., Saunders, C. et al. Mutation spectrum in patients with fructose-1,6-bisphosphatase deficiency. J Inherit Metab Dis 24, 87–88 (2001). https://doi.org/10.1023/A:1005691730058

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  • DOI: https://doi.org/10.1023/A:1005691730058

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