Novel heterozygous missense mutation of SLC12A3 gene in Gitelman syndrome: A case report

doi:10.12998/wjcc.v7.i12.1522

Advanced Search

BPG is committed to discovery and dissemination of knowledge

Home / Archive / Volume 7, Issue 12

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 (5529)

All Articles published online

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

Item

Count

PDF

341

WORD

176

HTML

2329

Figures (1-3)

538

Tables (1-3)

232

Sum=3616

Publishing Process of This Article

The chart showing Browse series, Download series.

Item

Count

Browse

637

Download

1276

Sum=1913

Jun 26, 2019 (publication date) through Nov 2, 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. Jun 26, 2019; 7(12): 1522-1528
Published online Jun 26, 2019. doi: 10.12998/wjcc.v7.i12.1522

Open in New Tab Full Size Figure Download Figure

Figure 1 Raw reads of exome sequencing.

Open in New Tab Full Size Figure Download Figure

Figure 2 Quality control results of exome sequencing.

Open in New Tab Full Size Figure Download Figure

Figure 3 Number of variants.

Citation: Wang CL. Novel heterozygous missense mutation of SLC12A3 gene in Gitelman syndrome: A case report. World J Clin Cases 2019; 7(12): 1522-1528
URL: https://www.wjgnet.com/2307-8960/full/v7/i12/1522.htm
DOI: https://dx.doi.org/10.12998/wjcc.v7.i12.1522