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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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