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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: ohba 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.
Dihydropyrimidinuria: the first case in Japan.
Ohba S, Kidouchi K, Sumi S, Imaeda M, Takeda N, Yoshizumi H, Tatematsu A, Kodama K, Yamanaka K, Kobayashi M, et al. Ohba S, et al. Adv Exp Med Biol. 1994;370:383-6. doi: 10.1007/978-1-4615-2584-4_83. Adv Exp Med Biol. 1994. PMID: 7660934 No abstract available.
Dihydropyrimidinuria without clinical symptoms.
Sumi S, Kidouchi K, Hayashi K, Ohba S, Wada Y. Sumi S, et al. Among authors: ohba s. J Inherit Metab Dis. 1996;19(5):701-2. doi: 10.1007/BF01799851. J Inherit Metab Dis. 1996. PMID: 8892031 No abstract available.
737 results