Mutation and Polymorphism Analysis of the Human Homogentisate 1,2-Dioxygenase Gene in Alkaptonuria Patients
- 1 April 1998
- journal article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 62 (4), 776-784
- https://doi.org/10.1086/301805
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- The Human Homogentisate 1,2-Dioxygenase (HGO) GeneGenomics, 1997
- Cloning of the homogentisate 1,2-dioxygenase gene, the key enzyme of alkaptonuria in mouseMammalian Genome, 1997
- Molecular defects in alkaptonuriaCytogenetic and Genome Research, 1997
- The molecular basis of alkaptonuriaNature Genetics, 1996
- Molecular Characterization of a Gene Encoding a Homogentisate Dioxygenase from Aspergillus nidulans and Identification of Its Human and Plant HomologuesPublished by Elsevier BV ,1995
- Mutation of human short tandem repeatsHuman Molecular Genetics, 1993
- Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms.Proceedings of the National Academy of Sciences, 1989
- THE NATURE OF THE DEFECT IN TYROSINE METABOLISM IN ALCAPTONURIAJournal of Biological Chemistry, 1958
- HOMOGENTISATE OXIDASE OF LIVERJournal of Biological Chemistry, 1955
- THE INCIDENCE OF ALKAPTONURIA : A STUDY IN CHEMICAL INDIVIDUALITY.The Lancet, 1902