| 1 | MCEE, MCEED
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| Atypical methylmalonic aciduria: frequency of mutations in the methylmalonyl CoA epimerase gene (MCEE).
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| Gradinger AB, Bélair C, Worgan LC, Li CD, Lavallée J, Roquis D, Watkins D, Rosenblatt DS.
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| Hum Mutat 28(10):1045.
2007
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| 2 | MCEE, MCEED
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| Homozygous nonsense mutation in the MCEE gene and siRNA suppression of methylmalonyl-CoA epimerase expression: a novel cause of mild methylmalonic aciduria.
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| Dobson CM, Gradinger A, Longo N, Wu X, Leclerc D, Lerner-Ellis J, Lemieux M, Belair C, Watkins D, Rosenblatt DS, Gravel RA.
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| Mol Genet Metab 88(4):327-33. Epub 2006 May 11. 2006
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| 3 | MCEE, MCEED
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| A homozygous nonsense mutation in the methylmalonyl-CoA epimerase gene (MCEE) results in mild methylmalonic aciduria.
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| Bikker H, Bakker HD, Abeling NG, Poll-The BT, Kleijer WJ, Rosenblatt DS, Waterham HR, Wanders RJ, Duran M.
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| Hum Mutat 27(7):640-3. 2006
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| 4 | MCEE
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| Identification of the human methylmalonyl-CoA racemase gene based on theanalysis of prokaryotic gene arrangements. Implications for decoding the humangenome.
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| Bobik TA, Rasche ME.
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| J Biol Chem 276(40):37194-8. 2001
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