Vitamin E Deficiency Familial Ataxic Syndrome
A total of 8 members of two consanguineous Tunisian families affected with Friedreich’s ataxia (FA) phenotype not linked to chromosome 9 were found to have very low levels of serum vitamin E (0.5 mcg/ml cf 8 mcg/ml in controls) in a study at the Institut National de Neurologie, Tunis, and at Centers...
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| Format: | Article |
| Language: | English |
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Pediatric Neurology Briefs Publishers
1993-12-01
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| Series: | Pediatric Neurology Briefs |
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| Online Access: | https://www.pediatricneurologybriefs.com/articles/2828 |