Friedreich-like ataxia with retinitis pigmentosa caused by the His101Gln mutation of the ?-Tocopherol transfer protein gene-Reference-Cited by-同舟云学术

Friedreich-like ataxia with retinitis pigmentosa caused by the His101Gln mutation of the ?-Tocopherol transfer protein gene

Published:1997-06 Issue:6 Volume:41 Page:826-832
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Yokota Takanori,Shiojiri Toshiaki,Gotoda Takanari,Arita Makoto,Arai Hiroyuki,Ohga Tatsuhide,Kanda Takashi,Suzuki Junichi,Imai Tomihiro,Matsumoto Hiroyuki,Harino Seiyo,Kiyosawa Motohiro,Mizusawa Hidehiro,Inoue Keizo

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference42 articles.

1. Absorption, lipoprotein transport, and regulation of plasma concentrations of vitamin E in humans.

2. Purification and characterization of the α-tocopherol transfer protein from rat liver

3. Identification, purification, and immunochemical characterization of a tocopherol-binding protein in rat liver cytosol.

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

5. Adult-onset spinocerebellar syndrome with idiopathic vitamin E deficiency

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