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A family study of congenital malabsorption of folate

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Journal of Inherited Metabolic Disease

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REFERENCES

  • Poncz M, Colman N, Herbert V, et al (1981) Therapy of congenital folate malabsorption. J Pediatr 98: 76-79.

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  • Zittoun J, Marquet J, Zittoun R (1978) Effect of folate and cobalamin compounds on the deoxyuridine suppression test in vitamin B12 and folate deficiency. Blood 51: 119-128.

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Authors and Affiliations

  1. Centre de Maternité et de Néonatologie de Tunis, 1007, El Jabri, Tunis, Tunisia

    S. Jebnoun, S. Kacem, Ch. Mokrani, A. Chabchoub & N. Khrouf

  2. Centre Hospitalier Intercommunal de Créteil, Paris, France

    J. Zittoun

Authors
  1. S. Jebnoun
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  2. S. Kacem
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  3. Ch. Mokrani
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  4. A. Chabchoub
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  5. N. Khrouf
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  6. J. Zittoun
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Jebnoun, S., Kacem, S., Mokrani, C. et al. A family study of congenital malabsorption of folate. J Inherit Metab Dis 24, 749–750 (2001). https://doi.org/10.1023/A:1012905823879

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  • DOI: https://doi.org/10.1023/A:1012905823879

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