✦ LIBER ✦
Isolated late-onset cone-rod dystrophy revealing a familial neurogenic muscle weakness, ataxia, and retinitis pigmentosa syndrome with the T8993G mitochondrial mutation
✍ Scribed by Fernanda B.O Porto; Geneviève Mack; Marie-Josèphe Sterboul; Patricia Lewin; Jacques Flament; José Sahel; Hélène Dollfus
- Book ID
- 117017981
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- English
- Weight
- 162 KB
- Volume
- 132
- Category
- Article
- ISSN
- 0002-9394
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