1. Baraitser M (1989) The genetics of the spinal muscular atrophies. Progr Clin Biol Res 306:75–84
2. Bassen FA, Kornzweig AL (1950) Malformation of the erythrocytes in a case of atypical retinitis pigmentosa. Blood 5:381–387
3. Ben Hamida M, Hentati F, Ben Hamida C (1990) Hereditary motor system diseases (chronic juvenile amyotrophic lateral sclerosis). Brain 113:347–363
4. Ben Hamida C, Doerflinger N, Belal S et al. (1993a) Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping. Nat Genet 5:195–200
5. Ben Hamida M, Belal S, Sirugo G et al. (1993b) Friedreich’s ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian families. Neurology 43:2179–2183