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Folates and homocystinuria

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Journal of Inherited Metabolic Disease

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References

  • Branda, R. F. and Anthony, B. K. Evidence for transfer of folate compounds by specialized erythrocyte membrane system.J. Lab. Clin. Med. 94 (1979) 354–360

    Google Scholar 

  • Kutzbach, C. and Stokstad, E. L. R. Mammalian methylene tetrahydrofolate reductase: partial purification, properties and inhibition byS-adenosylmethionine.Biochim. Biophys. Acta 250 (1971) 459–465

    Google Scholar 

  • Skovby, F. Homocystinuria: clinical, biochemical and genetic aspects of cystathionine-β-synthase and its deficiency in man.Acta Paediatr. Scand. Suppl. 321 (1985) 1–21

    Google Scholar 

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Ferraris, S., Bonetti, G., Biasetti, S. et al. Folates and homocystinuria. J Inherit Metab Dis 11, 310–311 (1988). https://doi.org/10.1007/BF01800380

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