Novel compound heterozygous GPR56 gene mutation in a twin with lissencephaly: A case report

doi:10.12998/wjcc.v10.i2.607

Advanced Search

BPG is committed to discovery and dissemination of knowledge

Home / Archive / Volume 10, Issue 2

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 (4380)

All Articles published online

The chart showing PDF series, WORD series, HTML series, Figures (1-2) series, Tables (1-1) series.

Item

Count

PDF

221

WORD

137

HTML

1673

Figures (1-2)

274

Tables (1-1)

381

Sum=2686

Featured Article

The chart showing Browse series, Download series.

Item

Count

Browse

254

Download

431

Sum=685

Publishing Process of This Article

Item

Count

Browse

267

Download

742

Sum=1009

Jan 14, 2022 (publication date) through Dec 25, 2024

Times Cited of This Article

Times Cited (2)

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 14, 2022; 10(2): 607-617
Published online Jan 14, 2022. doi: 10.12998/wjcc.v10.i2.607

Full Size Figure Download Figure

Figure 1 Brain magnetic resonance imaging of the proband revealed a simple brain structure, with widened and thickened gyri and shallow sulci.

Citation: Lin WX, Chai YY, Huang TT, Zhang X, Zheng G, Zhang G, Peng F, Huang YJ. Novel compound heterozygous GPR56 gene mutation in a twin with lissencephaly: A case report. World J Clin Cases 2022; 10(2): 607-617
URL: https://www.wjgnet.com/2307-8960/full/v10/i2/607.htm
DOI: https://dx.doi.org/10.12998/wjcc.v10.i2.607