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A new Japanese case of succinyl-CoA: 3-ketoacid CoA-transferase deficiency

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Journal of Inherited Metabolic Disease

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Sakazaki, H., Hirayama, K., Murakami, S. et al. A new Japanese case of succinyl-CoA: 3-ketoacid CoA-transferase deficiency. J Inherit Metab Dis 18, 323–325 (1995). https://doi.org/10.1007/BF00710423

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