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Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Garrod A. E. A Contribution to the Study of Alkaptonuria. Med Chir Trans. 1899;82:367–394. doi: 10.1177/095952879908200119. [DOI] [PMC free article] [PubMed] [Google Scholar]
- LA DU B. N., ZANNONI V. G., LASTER L., SEEGMILLER J. E. The nature of the defect in tyrosine metabolism in alcaptonuria. J Biol Chem. 1958 Jan;230(1):251–260. [PubMed] [Google Scholar]
- La Du B. N., Jr Alcaptonuria and ochronotic arthritis. Mol Biol Med. 1991 Feb;8(1):31–38. [PubMed] [Google Scholar]
- Menon I. A., Persad S. D., Haberman H. F., Basu P. K., Norfray J. F., Felix C. C., Kalyanaraman B. Characterization of the pigment from homogentisic acid and urine and tissue from an alkaptonuria patient. Biochem Cell Biol. 1991 Apr;69(4):269–273. doi: 10.1139/o91-041. [DOI] [PubMed] [Google Scholar]
- Montagutelli X., Lalouette A., Coudé M., Kamoun P., Forest M., Guénet J. L. aku, a mutation of the mouse homologous to human alkaptonuria, maps to chromosome 16. Genomics. 1994 Jan 1;19(1):9–11. doi: 10.1006/geno.1994.1004. [DOI] [PubMed] [Google Scholar]
- Pollak M. R., Chou Y. H., Cerda J. J., Steinmann B., La Du B. N., Seidman J. G., Seidman C. E. Homozygosity mapping of the gene for alkaptonuria to chromosome 3q2. Nat Genet. 1993 Oct;5(2):201–204. doi: 10.1038/ng1093-201. [DOI] [PubMed] [Google Scholar]