Neurodegeneration bei Vitamin-E-Mangel
Author:
Publisher
Springer Science and Business Media LLC
Subject
Materials Chemistry
Link
http://link.springer.com/article/10.1007/s42451-018-0020-8/fulltext.html
Reference12 articles.
1. Hamida BM, Belal S, Sirugo G et al (1993) Friedreich’s ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in to inbred Tunsian families. Neurology 43:2179–2183
2. Hamida BC, Doerflinger N, Belal S et al (1993) Localisation of Friedreich ataxia phenoype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping. Nat Genet 5:195–200
3. Burck U, Goebel HH, Kuhlendahl HD et al (1981) Neuromyopathy and vitamin E deficiency in man. Neuropediatrics 12:267–278
4. Cavalier L, Ouachi K, Kayden HJ et al (1998) Ataxia with isolated vitamin E deficiency: heterogeneity of mutations and phenotypic variability in a large number of families. Am J Hum Genet 68:301–310
5. Delatycki MB, Williamson R, Forrest SM (2000) Friedreich ataxia: an overview. J Med Genet 37:1–8
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