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Results: 1-1 |
Results: 1
Isolated late-onset cone-rod dystrophy revealing a familial neurogenic muscle weakness, ataxia, and retinitis pigmentosa syndrome with the T8993G mitochondrial mutation
Authors: Porto, FBO Mack, G Sterboul, MP Lewin, P Flament, J Sahel, J Dollfus, H
Citation: Fbo. Porto et al., Isolated late-onset cone-rod dystrophy revealing a familial neurogenic muscle weakness, ataxia, and retinitis pigmentosa syndrome with the T8993G mitochondrial mutation, AM J OPHTH, 132(6), 2001, pp. 935-937
Risultati: 1-1 |