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Results: 1-5 |
Results: 5

Authors: Darin, N Oldfors, A Moslemi, AR Holme, E Tulinius, M
Citation: N. Darin et al., The incidence of mitochondrial encephalomyopathies in childhood: Clinical features and morphological, biochemical, and DNA abnormalities, ANN NEUROL, 49(3), 2001, pp. 377-383

Authors: Darin, N Tulinius, M
Citation: N. Darin et M. Tulinius, Neuromuscular disorders in childhood: a descriptive epidemiological study from western Sweden, NEUROMUSC D, 10(1), 2000, pp. 1-9

Authors: Martinsson, T Oldfors, A Darin, N Berg, K Tajsharghi, H Kyllerman, M Wahlstrom, J
Citation: T. Martinsson et al., Autosomal dominant myopathy: Missense mutation (Glu-706 -> Lys) in the myosin heavy chain IIa gene, P NAS US, 97(26), 2000, pp. 14614-14619

Authors: Jansson, M Darin, N Kyllerman, M Martinsson, T Wahlstrom, J Oldfors, A
Citation: M. Jansson et al., Multiple mitochondrial DNA deletions in hereditary inclusion body myopathy, ACT NEUROP, 100(1), 2000, pp. 23-28

Authors: Martinsson, T Darin, N Kyllerman, M Oldfors, A Hallberg, B Wahlstrom, J
Citation: T. Martinsson et al., Dominant hereditary inclusion-body myopathy gene (IBM3) maps to chromosomeregion 17p13.1, AM J HU GEN, 64(5), 1999, pp. 1420-1426
Risultati: 1-5 |