Novel α-galactosidase A gene mutation in a Chinese Fabry disease family: A case report

doi:10.12998/wjcc.v10.i3.1067

Advanced Search

BPG is committed to discovery and dissemination of knowledge

Home / Archive / Volume 10, Issue 3

This Article

Academic Content and Language Evaluation 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 (2843)

All Articles published online

The chart showing PDF series, WORD series, HTML series, Figures (1-8) series, Tables (1-1) series.

Item

Count

PDF

200

WORD

191

HTML

1368

Figures (1-8)

293

Tables (1-1)

220

Sum=2272

Publishing Process of This Article

The chart showing Browse series, Download series.

Item

Count

Browse

223

Download

348

Sum=571

Jan 21, 2022 (publication date) through Apr 26, 2024

Times Cited of This Article

Times Cited (0)

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. Jan 21, 2022; 10(3): 1067-1076
Published online Jan 21, 2022. doi: 10.12998/wjcc.v10.i3.1067

Full Size Figure Download Figure

Figure 4 Light microscopy of renal biopsy (periodic acid-Schiff staining, 400 ×) showing membranous nephropathy. Heterogeneous thickening of the glomerular capillary basement membrane is visible.

Citation: Fu AY, Jin QZ, Sun YX. Novel α-galactosidase A gene mutation in a Chinese Fabry disease family: A case report. World J Clin Cases 2022; 10(3): 1067-1076
URL: https://www.wjgnet.com/2307-8960/full/v10/i3/1067.htm
DOI: https://dx.doi.org/10.12998/wjcc.v10.i3.1067