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Intrafamilial phenotypic variability in citrullinaemia: Report of a family

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Journal of Inherited Metabolic Disease

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References

  • Kennaway, N. G., Harwood, P. J., Ramberg, D. A., Koler, R. D. and Buist, N. R. M. Citrullinemia: Enzymatic evidence for genetic heterogeneity.Pediatr. Res. 9 (1975) 554–558

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Authors and Affiliations

  1. KUWAIT Paediatric Department, Clinical Biochemistry Department, Sabah Hospital and Medical Genetics Centre, Maternity Hospital, P.O. Box: 36660 Raas, 24757, Kuwait

    A. S. Teebi

Authors
  1. A. R. A. Issa
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  2. G. Yadav
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  3. A. S. Teebi
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Issa, A.R.A., Yadav, G. & Teebi, A.S. Intrafamilial phenotypic variability in citrullinaemia: Report of a family. J Inherit Metab Dis 11, 306–307 (1988). https://doi.org/10.1007/BF01800377

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  • DOI: https://doi.org/10.1007/BF01800377

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