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Journal of the Neurological Sciences
Volume 198, Issue 1
, Pages 25-29
, 15 June 2002
Clinical comparison between AVED patients with 744 del A mutation and Friedreich ataxia with GAA expansion in 15 Moroccan families
References
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- (a) Friedeich's ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian families. Neurology. 1993;43:2179–2183 (b) Localisation of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping. Nat. Genet. 1993;5:195–200
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PII: S0022-510X(02)00057-6
© 2002 Elsevier Science B.V. All rights reserved.
« Previous
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Journal of the Neurological Sciences
Volume 198, Issue 1
, Pages 25-29
, 15 June 2002
