. . . . . . . "[Ataxia with vitamin E deficiency is an autosomal recessive cerebellar ataxia caused by mutations in the ?-tocopherol transfer protein coding gene localized on chromosome 8q, leading to lower levels of serum vitamin E. More than 91 patients diagnosed with ataxia with vitamin E deficiency have been reported worldwide.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2017-02-19"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2017-10-17T13:17:05+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .