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Results: 1-4 |
Results: 4
Eight novel mutations and consequences on mRNA and protein level in pyruvate kinase-deficient patients with nonspherocytic hemolytic anemia
Authors: Kugler, W Willaschek, C Holtz, C Ohlenbusch, A Laspe, P Krugener, R Muirhead, H Schroter, W Lakomek, M
Citation: W. Kugler et al., Eight novel mutations and consequences on mRNA and protein level in pyruvate kinase-deficient patients with nonspherocytic hemolytic anemia, HUM MUTAT, 15(3), 2000, pp. 261-272
Genospecies diversity of Lyme disease spirochetes in rodent reservoirs
Authors: Richter, D Endepols, S Ohlenbusch, A Eiffert, H Spielman, A Matuschka, FR
Citation: D. Richter et al., Genospecies diversity of Lyme disease spirochetes in rodent reservoirs, EM INFECT D, 5(2), 1999, pp. 291-296
Characterization of the mitochondrial genome in childhood multiple sclerosis II. Multiple sclerosis without optic neuritis and LHON-associated genes
Authors: Wilichowski, E Ohlenbusch, A Hanefeld, F
Citation: E. Wilichowski et al., Characterization of the mitochondrial genome in childhood multiple sclerosis II. Multiple sclerosis without optic neuritis and LHON-associated genes, NEUROPEDIAT, 29(6), 1998, pp. 307-312
Characterization of the mitochondrial genome in childhood multiple sclerosis III. Multiple sclerosis without optic neuritis and the non-LHON-associated genes
Authors: Ohlenbusch, A Wilichowski, E Hanefeld, F
Citation: A. Ohlenbusch et al., Characterization of the mitochondrial genome in childhood multiple sclerosis III. Multiple sclerosis without optic neuritis and the non-LHON-associated genes, NEUROPEDIAT, 29(6), 1998, pp. 313-319
Risultati: 1-4 |