Isolated late-onset cone-rod dystrophy revealing a familial neurogenic muscle weakness, ataxia, and retinitis pigmentosa syndrome with the T8993G mitochondrial mutation
- DOI
- 10.1016/s0002-9394(01)01187-4
- Published
- 2001-12
- Container
- American Journal of Ophthalmology
- Publisher
- Elsevier BV
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1016/s0002-9394-01-01187-4,
title = {Isolated late-onset cone-rod dystrophy revealing a familial neurogenic muscle weakness, ataxia, and retinitis pigmentosa syndrome with the T8993G mitochondrial mutation},
author = {Fernanda B.O Porto and Geneviève Mack and Marie-Josèphe Sterboul and Patricia Lewin and Jacques Flament and José Sahel and Hélène Dollfus},
year = {2001},
journal = {American Journal of Ophthalmology},
doi = {10.1016/s0002-9394(01)01187-4},
url = {https://doi.org/10.1016/s0002-9394(01)01187-4}
}RIS
TY - JOUR TI - Isolated late-onset cone-rod dystrophy revealing a familial neurogenic muscle weakness, ataxia, and retinitis pigmentosa syndrome with the T8993G mitochondrial mutation AU - Fernanda B.O Porto AU - Geneviève Mack AU - Marie-Josèphe Sterboul AU - Patricia Lewin AU - Jacques Flament AU - José Sahel AU - Hélène Dollfus PY - 2001 JO - American Journal of Ophthalmology DO - 10.1016/s0002-9394(01)01187-4 UR - https://doi.org/10.1016/s0002-9394(01)01187-4 ER -
APA
Porto, F. B., Mack, G., Sterboul, M., Lewin, P., Flament, J., Sahel, J., & Dollfus, H. (2001). Isolated late-onset cone-rod dystrophy revealing a familial neurogenic muscle weakness, ataxia, and retinitis pigmentosa syndrome with the T8993G mitochondrial mutation. American Journal of Ophthalmology. https://doi.org/10.1016/s0002-9394(01)01187-4
Source records
- crossref · retrieved 2026-09-25T23:05:39.541Z