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Molecular mechanism of a temperature-sensitive phenotype in peroxisomal biogenesis disorder.
Hashimoto K, Kato Z, Nagase T, Shimozawa N, Kuwata K, Omoya K, Li A, Matsukuma E, Yamamoto Y, Ohnishi H, Tochio H, Shirakawa M, Suzuki Y, Wanders RJ, Kondo N. Hashimoto K, et al. Among authors: suzuki y. Pediatr Res. 2005 Aug;58(2):263-9. doi: 10.1203/01.PDR.0000169984.89199.69. Epub 2005 Jul 8. Pediatr Res. 2005. PMID: 16006427 Free article.
Peroxisomal acyl CoA oxidase deficiency.
Suzuki Y, Iai M, Kamei A, Tanabe Y, Chida S, Yamaguchi S, Zhang Z, Takemoto Y, Shimozawa N, Kondo N. Suzuki Y, et al. J Pediatr. 2002 Jan;140(1):128-30. doi: 10.1067/mpd.2002.120511. J Pediatr. 2002. PMID: 11815777
A PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parents.
Raas-Rothschild A, Wanders RJ, Mooijer PA, Gootjes J, Waterham HR, Gutman A, Suzuki Y, Shimozawa N, Kondo N, Eshel G, Espeel M, Roels F, Korman SH. Raas-Rothschild A, et al. Among authors: suzuki y. Am J Hum Genet. 2002 Apr;70(4):1062-8. doi: 10.1086/339766. Epub 2002 Feb 28. Am J Hum Genet. 2002. PMID: 11873320 Free PMC article.
Epidemiology of X-linked adrenoleukodystrophy in Japan.
Takemoto Y, Suzuki Y, Tamakoshi A, Onodera O, Tsuji S, Hashimoto T, Shimozawa N, Orii T, Kondo N. Takemoto Y, et al. Among authors: suzuki y. J Hum Genet. 2002;47(11):590-3. doi: 10.1007/s100380200090. J Hum Genet. 2002. PMID: 12436195
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