![](/img/cover-not-exists.png)
Isolated late-onset cone-rod dystrophy revealing a familial neurogenic muscle weakness, ataxia, and retinitis pigmentosa syndrome with the T8993G mitochondrial mutation
Fernanda B.O Porto, Geneviève Mack, Marie-Josèphe Sterboul, Patricia Lewin, Jacques Flament, José Sahel, Hélène DollfusVolume:
132
Year:
2001
Language:
english
DOI:
10.1016/s0002-9394(01)01187-4
File:
PDF, 162 KB
english, 2001