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Mol Med. 1996 May; 2(3): 271–273.
PMCID: PMC2230147

Inborn errors of metabolism: Garrod's legacy.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.
  • Garrod AE. A Contribution to the Study of Alkaptonuria. Med Chir Trans. 1899;82:367–394. [PMC free article] [PubMed]
  • Menon IA, Persad SD, Haberman HF, Basu PK, Norfray JF, Felix CC, 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. [PubMed]
  • LA DU BN, ZANNONI VG, LASTER L, SEEGMILLER JE. The nature of the defect in tyrosine metabolism in alcaptonuria. J Biol Chem. 1958 Jan;230(1):251–260. [PubMed]
  • Montagutelli X, Lalouette A, Coudé M, Kamoun P, Forest M, Guénet JL. aku, a mutation of the mouse homologous to human alkaptonuria, maps to chromosome 16. Genomics. 1994 Jan 1;19(1):9–11. [PubMed]
  • Pollak MR, Chou YH, Cerda JJ, Steinmann B, La Du BN, Seidman JG, Seidman CE. Homozygosity mapping of the gene for alkaptonuria to chromosome 3q2. Nat Genet. 1993 Oct;5(2):201–204. [PubMed]
  • La Du BN., Jr Alcaptonuria and ochronotic arthritis. Mol Biol Med. 1991 Feb;8(1):31–38. [PubMed]

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