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Items where Author is "Maier, E"

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Article

Maier, EM, Mayerhofer, PU, Asheuer, M, Kohler, W, Rothe, M, Muntau, AC, Roscher, AA, Holzinger, A, Aubourg, P and Berger, J (2008) X-linked adrenoleukodystrophy phenotype is independent of ABCD2 genotype Biochem Biophys Res Commun, 377. pp. 176-180.

Stadler, SC, Polanetz, R, Maier, EM, Heidenreich, SC, Niederer, B, Mayerhofer, PU, Lagler, F, Koch, HG, Santer, R, Fletcher, JM, Ranieri, E, Das, AM, Spiekerkotter, U, Schwab, KO, Potzsch, S, Marquardt, I, Hennermann, JB, Knerr, I, Mercimek-Mahmutoglu, S, Kohlschmidt, N, Liebl, B, Fingerhut, R, Olgemoller, B, Muntau, AC, Roscher, AA and Roschinger, W (2006) Newborn screening for 3-methylcrotonyl-CoA carboxylase deficiency: population heterogeneity of MCCA and MCCB mutations and impact on risk assessment Hum Mutat, 27. pp. 748-759.

Holzinger, A, Maier, EM, Buck, C, Mayerhofer, PU, Kappler, M, Haworth, JC, Moroz, SP, Hadorn, HB, Sadler, JE and Roscher, AA (2002) Mutations in the proenteropeptidase gene are the molecular cause of congenital enteropeptidase deficiency Am J Hum Genet, 70. pp. 20-25.

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