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. 1990 Jun 9;300(6738):1512–1514. doi: 10.1136/bmj.300.6738.1512

An independent diagnosis.

PMCID: PMC1663185 PMID: 2372606

1512

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

Cross N. C., Tolan D. R., Cox T. M. Catalytic deficiency of human aldolase B in hereditary fructose intolerance caused by a common missense mutation. Cell. 1988 Jun 17;53(6):881–885. doi: 10.1016/s0092-8674(88)90349-2. [DOI] [PubMed] [Google Scholar]
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