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Results: 1-5 |
Results: 5

Authors: Absalon, MJ Harding, CO Fain, DR Li, L Mack, KJ
Citation: Mj. Absalon et al., Leigh syndrome in an infant resulting from mitochondrial DNA depletion, PED NEUROL, 24(1), 2001, pp. 60-63

Authors: Harding, CO
Citation: Co. Harding, 'Mommy, why can't I have a hamburger like the other kids?', GENE THER, 7(23), 2000, pp. 1969-1970

Authors: Wolff, JA Harding, CO
Citation: Ja. Wolff et Co. Harding, Principles of gene therapy for inborn errors of metabolism, GENE THERAPY, 2000, pp. 507-518

Authors: Jean, JC Harding, CO Oakes, SM Yu, Q Held, PK Joyce-Brady, M
Citation: Jc. Jean et al., gamma-Glutamyl transferase (GGT) deficiency in the GGT(enu1) mouse resultsfrom a single point mutation that leads to a stop codon in the first coding exon of GGT mRNA, MUTAGENESIS, 14(1), 1999, pp. 31-36

Authors: Harding, CO Gillingham, MB van Calcar, SC Wolff, JA Verhoeve, JN Mills, MD
Citation: Co. Harding et al., Docosahexaenoic acid and retinal function in children with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency, J INH MET D, 22(3), 1999, pp. 276-280
Risultati: 1-5 |