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Page 1
Pyrimidine metabolism in hereditary orotic aciduria.
Sumi S, Suchi M, Kidouchi K, Morishita H, Ohba S, Wada Y. Sumi S, et al. J Inherit Metab Dis. 1997 Mar;20(1):104-5. doi: 10.1023/a:1005330127995. J Inherit Metab Dis. 1997. PMID: 9061575 No abstract available.
Dihydropyrimidinase deficiency: structural organization, chromosomal localization, and mutation analysis of the human dihydropyrimidinase gene.
Hamajima N, Kouwaki M, Vreken P, Matsuda K, Sumi S, Imaeda M, Ohba S, Kidouchi K, Nonaka M, Sasaki M, Tamaki N, Endo Y, De Abreu R, Rotteveel J, van Kuilenburg A, van Gennip A, Togari H, Wada Y. Hamajima N, et al. Among authors: sumi s. Am J Hum Genet. 1998 Sep;63(3):717-26. doi: 10.1086/302022. Am J Hum Genet. 1998. PMID: 9718352 Free PMC article.
[Purine nucleoside phosphorylase (PNP) deficiency].
Sumi S, Wada Y. Sumi S, et al. Ryoikibetsu Shokogun Shirizu. 1998;(18 Pt 1):458-9. Ryoikibetsu Shokogun Shirizu. 1998. PMID: 9590100 Review. Japanese. No abstract available.
[Pyrimidine-5'-nucleotidase deficiency].
Sumi S, Wada Y. Sumi S, et al. Ryoikibetsu Shokogun Shirizu. 1998;(18 Pt 1):487-9. Ryoikibetsu Shokogun Shirizu. 1998. PMID: 9590109 Review. Japanese. No abstract available.
481 results