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Human Genetics|March 1, 1991
Genotype-phenotype relationship in various degrees of arylsulfatase A deficiencyJ Kappler, P Leinekugel, E Conzelmann, et al.Pediatric Research|November 1, 1985
Prenatal diagnosis of GM2 gangliosidosis with high residual hexosaminidase A activity (variant B1; pseudo AB variant)E Conzelmann, H Nehrkorn, H J Kytzia, et al.American Journal of Medical Genetics|September 5, 1997
Leukodystrophy incidence in GermanyP Heim, M Claussen, B Hoffmann, et al.The Journal of Biological Chemistry|April 20, 2000
In mouse alpha -methylacyl-CoA racemase, the same gene product is simultaneously located in mitochondria and peroxisomesT J Kotti, K Savolainen, H M Helander, et al.The Biochemical Journal|January 1, 1997
Peroxisomal multifunctional enzyme of beta-oxidation metabolizing D-3-hydroxyacyl-CoA esters in rat liver: molecular cloning, expression and characterizationY M Qin, M H Poutanen, H M Helander, et al.Pageof 5