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A case of 2-methylacetoacetyl CoA thiolase deficiency with coincidental chromosome abnormalities.

Gray RG, Lowther GW, Littlewood JM, Middleton B, Bennett MJ. A case of 2-methylacetoacetyl CoA thiolase deficiency with coincidental chromosome abnormalities. J Med Genet. 1984 Oct; 21(5):397.

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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.