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Genomics|June 1, 1992
Strand-separating conformational polymorphism analysis: efficacy of detection of point mutations in the human ornithine delta-aminotransferase geneJ Michaud, L C Brody, G Steel, et al.The Journal of Biological Chemistry|February 15, 1992
Ornithine delta-aminotransferase mutations in gyrate atrophy. Allelic heterogeneity and functional consequencesL C Brody, G A Mitchell, C Obie, et al.American Journal of Human Genetics|March 1, 1995
Pyridoxine-responsive gyrate atrophy of the choroid and retina: clinical and biochemical correlates of the mutation A226VJ Michaud, G N Thompson, L C Brody, et al.The Journal of Biological Chemistry|October 5, 1988
Human ornithine-delta-aminotransferase. cDNA cloning and analysis of the structural geneG A Mitchell, J E Looney, L C Brody, et al.The Journal of Clinical Investigation|February 1, 1988
An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy of the choroid and retinaG A Mitchell, L C Brody, J Looney, et al.Human Molecular Genetics|November 1, 1993
Expression and processing of human ornithine-delta-aminotransferase in Saccharomyces cerevisiaeK M Dougherty, D A Swanson, L C Brody, et al.Genomics|May 1, 1993
The isolation of cDNAs from OATL1 at Xp 11.2 using a 480-kb YACM T Geraghty, L C Brody, L S Martin, et al.Proceedings of the National Academy of Sciences of the United States of America|February 1, 1991
Splice-mediated insertion of an Alu sequence inactivates ornithine delta-aminotransferase: a role for Alu elements in human mutationG A Mitchell, D Labuda, G Fontaine, et al.Human Genetics|May 1, 1992
Phenotype of disease in three patients with identical mutations in methylmalonyl CoA mutaseA M Crane, L S Martin, D Valle, et al.Clinical Genetics|September 7, 2005
Population history and its impact on medical genetics in QuebecA-M Laberge, J Michaud, A Richter, et al.Pageof 55