Gerstmann-Sträussler-Scheinker disease: A case report

doi:10.12998/wjcc.v7.i3.389

Advanced Search

BPG is committed to discovery and dissemination of knowledge

Home / Archive / Volume 7, Issue 3

This Article

Academic Content and Language Evaluation of This Article

CrossCheck and Google Search of This Article

Academic Rules and Norms of This Article

Supplementary Materials 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 (9345)

All Articles published online

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

Item

Count

PDF

352

WORD

301

HTML

5377

Figures (1-3)

379

Sum=6409

Publishing Process of This Article

The chart showing Browse series, Download series.

Item

Count

Browse

1119

Download

1817

Sum=2936

Feb 6, 2019 (publication date) through Dec 22, 2024

Times Cited of This Article

Times Cited (6)

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. Feb 6, 2019; 7(3): 389-395
Published online Feb 6, 2019. doi: 10.12998/wjcc.v7.i3.389

Full Size Figure Download Figure

Figure 2 Gene mapping of the proband. A heterozygous mutation site was found in the 2^nd exonic sequence of the PRNP gene (c.305; cytosine to thymine), resulting in a p.P102L amino acid change (valine to leucine).

Citation: Zhao MM, Feng LS, Hou S, Shen PP, Cui L, Feng JC. Gerstmann-Sträussler-Scheinker disease: A case report. World J Clin Cases 2019; 7(3): 389-395
URL: https://www.wjgnet.com/2307-8960/full/v7/i3/389.htm
DOI: https://dx.doi.org/10.12998/wjcc.v7.i3.389