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. 1970 Jun;63(6):605–606.

Familial hypercarotinaemia and hypovitaminosis A.

PMCID: PMC1811589 PMID: 5453458

605

Selected References

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

Brady R. O., Gal A. E., Bradley R. M., Martensson E., Warshaw A. L., Laster L. Enzymatic defect in Fabry's disease. Ceramidetrihexosidase deficiency. N Engl J Med. 1967 May 25;276(21):1163–1167. doi: 10.1056/NEJM196705252762101. [DOI] [PubMed] [Google Scholar]
Frenk E. Etat kératodermique avec taux sérique abaissé de la vitamine A et hypercarotinémie. Dermatologica. 1966;132(2):96–98. [PubMed] [Google Scholar]

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