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. 1977 Jul 9;2(6079):127. doi: 10.1136/bmj.2.6079.127-a

Diagnosing familial hypercholesterolaemia in childhood.

D J Betteridge, D Galton, M Giggins

PMCID: PMC1631013 PMID: 871792

127

Selected References

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

Betteridge D. J., Higgins M. J., Galton D. J. Regulation of 3-hydroxy-3-methylglutaryl coenzyme-A reductase activity in type II hyperlipoproteinaemia. Br Med J. 1975 Nov 29;4(5995):500–502. doi: 10.1136/bmj.4.5995.500. [DOI] [PMC free article] [PubMed] [Google Scholar]
Brown M. S., Goldstein J. L. Familial hypercholesterolemia: A genetic defect in the low-density lipoprotein receptor. N Engl J Med. 1976 Jun 17;294(25):1386–1390. doi: 10.1056/NEJM197606172942509. [DOI] [PubMed] [Google Scholar]

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