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Article

Familial ataxia with isolated vitamin E deficiency not due to mutation of alpha-TTP.

Journal of neurology - 1 Oct 1999

Shiojiri T, Yokota T, Fujimori N, Mizusawa H

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 10552255
DOI: 10.1007/s004150050499

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Familial ataxia with isolated vitamin E deficiency not due to mutation of alpha-TTP.PMID 10552255Read ↗

A novel delins mutation in the alpha-TTP gene in a family segregating ataxia with isolated vitamin E deficiency.Semantic proximity Read ↗

Ataxia with isolated vitamin E deficiency: heterogeneity of mutations and phenotypic variability in a large number of families.Semantic proximity Read ↗

A first description of ataxia with vitamin E deficiency associated with MT-TG gene mutation.Semantic proximity Read ↗

Pearls & Oy-sters: A Novel Presentation of Ataxia With Vitamin E Deficiency Caused by TTPA Gene Mutation.Semantic proximity Read ↗

Ataxia with vitamin E deficiency: update of molecular diagnosisSemantic proximity Read ↗

Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPA gene in Italian families.Semantic proximity Read ↗

Ataxia With Vitamin E Deficiency: Case Series, Vitamin E Therapy Response, Founder Effect, and In Silico Analysis.Semantic proximity Read ↗

Clinical and Genetic Study of Ataxia With Vitamin E DeficiencySemantic proximity Read ↗

Vitamin E deficiency ataxia with (744 del A) mutation on alpha-TTP gene: genetic and clinical peculiarities in Moroccan patients.Semantic proximity Read ↗

Ataxia caused by mutations in the alpha-tocopherol transfer protein gene.Semantic proximity Read ↗

Ataxia with vitamin E deficiency and severe dystonia: report of a case.Semantic proximity Read ↗

Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer protein.Semantic proximity Read ↗

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