Exacerbation of the ochronosis of alkaptonuria due to renal insufficiency and improvement after renal transplantation-Reference-Cited by-同舟云学术

Exacerbation of the ochronosis of alkaptonuria due to renal insufficiency and improvement after renal transplantation

Published:2002-09 Issue:1-2 Volume:77 Page:136-142
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Introne Wendy J,Phornphutkul Chanika,Bernardini Isa,McLaughlin Kevin,Fitzpatrick Diana,Gahl William A

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference15 articles.

1. B.N. La Du, Alkaptonuria, in: C.R. Scriver, A. Beaudet,W. Sly, D. Valle (Eds.), The Metabolic and Molecular Bases of Inherited Disease, vol. 2, eigth ed., McGraw-Hill, New York, 2001, pp. 2109–2123

2. The nature of the defect in tyrosine metabolism in alkaptonuria;La Du;J. Biol Chem,1958

3. The molecular basis of alkaptonuria;Fernandez-Canon;Nat. Genet.,1996

4. The human homogentisate 1,2-dioxygenase (HGO) gene;Granadino;Genomics,1997

5. Mutation and polymorphism analysis of the human homogentisate 1,2-dioxygenase gene in alkaptonuria patients;Beltran-Valero de Bernabe;Am. J. Hum. Genet.,1998

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