Friedreich's ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian families (fr)
Ataxia with isolated vitamin E deficiency is caused by mutations in the α-tocopherol transfer protein (fr)
Severe childhood muscular dystrophy affecting both sexes and frequent in Tunisia (fr)
Multiple cranial nerve deficits associated with the Arnold‐Chiari malformation (fr)