Cited by

• Mevalonate kinase assay using DEAE-cellulose column chromatography for first-trimester prenatal diagnosis and complementation analysis in mevalonic aciduria.

  Hoffmann GF, Brendel SU, Scharfschwerdt SR, Shin YS, Speidel IM, Gibson KM. Hoffmann GF, et al. J Inherit Metab Dis. 1992;15(5):738-46. doi: 10.1007/BF01800016. J Inherit Metab Dis. 1992. PMID: 1331607
• Long-term outcome in 134 patients with galactosaemia.

  Schweitzer S, Shin Y, Jakobs C, Brodehl J. Schweitzer S, et al. Eur J Pediatr. 1993 Jan;152(1):36-43. doi: 10.1007/BF02072514. Eur J Pediatr. 1993. PMID: 8444204
• A genetic factor for age-related cataract: identification and characterization of a novel galactokinase variant, "Osaka," in Asians.

  Okano Y, Asada M, Fujimoto A, Ohtake A, Murayama K, Hsiao KJ, Choeh K, Yang Y, Cao Q, Reichardt JK, Niihira S, Imamura T, Yamano T. Okano Y, et al. Am J Hum Genet. 2001 Apr;68(4):1036-42. doi: 10.1086/319512. Epub 2001 Feb 23. Am J Hum Genet. 2001. PMID: 11231902 Free PMC article.
• Red blood cell sorbitol dehydrogenase deficiency in a family with cataracts.

  Vaca G, Ibarra B, Bracamontes M, García-Cruz D, Sánchez-Corona J, Medina C, Wunsch C, González-Quiroga G, Cantú JM. Vaca G, et al. Hum Genet. 1982;61(4):338-41. doi: 10.1007/BF00276598. Hum Genet. 1982. PMID: 7152518
• Screening of the Philadelphia variant of galactokinase in racially unmixed black Africans: first results.

  Soni T, Brivet M, Blanc M, Jaeger G, Lemonnier A. Soni T, et al. Am J Hum Genet. 1988 Jan;42(1):96-103. Am J Hum Genet. 1988. PMID: 3422128 Free PMC article.