Clinical and genetic study of ataxia with vitamin E deficiency: A case report

doi:10.12998/wjcc.v10.i23.8271

Advanced Search

BPG is committed to discovery and dissemination of knowledge

Home / Archive / Volume 10, Issue 23

This Article

Academic Content and Language Evaluation of This Article

CrossCheck and Google Search of This Article

Academic Rules and Norms of This Article

Citation of this article

Corresponding Author of This Article

Research Domain of This Article

Article-Type of This Article

Open-Access Policy of This Article

Times Cited Counts in Google of This Article

Number of Hits and Downloads for This Article

Total Article Views (3652)

All Articles published online

The chart showing PDF series, WORD series, HTML series, Figures (1-3) series.

Item

Count

PDF

174

WORD

HTML

2436

Figures (1-3)

320

Sum=2994

Publishing Process of This Article

The chart showing Browse series, Download series.

Item

Count

Browse

176

Download

482

Sum=658

Aug 16, 2022 (publication date) through Dec 24, 2024

Times Cited of This Article

Times Cited (5)

Journal Information of This Article

Publication Name

World Journal of Clinical Cases

ISSN

2307-8960

Publisher of This Article

Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

Case Report

World J Clin Cases. Aug 16, 2022; 10(23): 8271-8276
Published online Aug 16, 2022. doi: 10.12998/wjcc.v10.i23.8271

Full Size Figure Download Figure

Figure 3 Evaluation of the mutation p. Arg301Gln is highly conserved among species.

Citation: Zhang LW, Liu B, Peng DT. Clinical and genetic study of ataxia with vitamin E deficiency: A case report. World J Clin Cases 2022; 10(23): 8271-8276
URL: https://www.wjgnet.com/2307-8960/full/v10/i23/8271.htm
DOI: https://dx.doi.org/10.12998/wjcc.v10.i23.8271