A Case of Ataxia with Isolated Vitamin E Deficiency Initially Diagnosed as Friedreich's Ataxia.

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A Case of Ataxia with Isolated Vitamin E Deficiency Initially Diagnosed as Friedreich's Ataxia.

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2016 nî lūn-bûn

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2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

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2016年论文

@zh

2016年论文

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A Case of Ataxia with Isolated ...... gnosed as Friedreich's Ataxia.

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Item

label

A Case of Ataxia with Isolated ...... gnosed as Friedreich's Ataxia.

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prefLabel

A Case of Ataxia with Isolated ...... gnosed as Friedreich's Ataxia.

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P1476

A Case of Ataxia with Isolated ...... gnosed as Friedreich's Ataxia.

@en

P2093

Michael Bonello

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Partha Ray

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P2860

The molecular basis of vitamin E retention: structure of human alpha-tocopherol transfer protein

Ataxia with vitamin E deficiency and abetalipoproteinemia.

Impaired ability of patients with familial isolated vitamin E deficiency to incorporate alpha-tocopherol into lipoproteins secreted by the liver.

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

Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping.

Ataxia with isolated vitamin E deficiency presenting as mutation negative Friedreich's ataxia.

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

Friedreich's ataxia with isolated vitamin E deficiency: a neuropathological study of a Tunisian patient.

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

Postmortem study of ataxia with retinitis pigmentosa by mutation of the alpha-tocopherol transfer protein gene.

P304

8342653

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P31

scholarly article

P356

10.1155/2016/8342653

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P478

2016

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P577

2016-02-16T00:00:00Z

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P5875

295094683

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P698

26989534

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P921

vitamin deficiency

P932

4771890

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