Friedrich's ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian families

• Published in: Neurology Vol. 43; no. 11; pp. 2179 - 2183
• Main Authors: BEN HAMIDA, M, BELAL, S, MIDDLETON, L, SIRUGO, G, BEN HAMIDA, C, PANAYIDES, K, IONANNOU, P, BECKMANN, J, MANDEL, J. L, HENTATI, F, KOENIG, M
• Format: Journal Article
• Language: English
• Published: Hagerstown, MD Lippincott Williams & Wilkins 1993
• Subjects: Biological and medical sciences; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases; Medical sciences; Neurology; Africa; Tunisia; Human; Nervous system diseases; Linkage; Family study; Deficiency; Vitamin; α-Tocopherol; Cerebral disorder; Genetic disease; C9-Chromosome; Phenotype; Central nervous system disease; Genetics; Degenerative disease; Consanguinity; Friedreich ataxia; Molecular biology; Spinal cord disease
• ISSN: 0028-3878; 1526-632X