Missense mutation in DYNC1H1 gene caused psychomotor developmental delay and muscle weakness: A case report

doi:10.12998/wjcc.v9.i30.9302

Advanced Search

BPG is committed to discovery and dissemination of knowledge

Home / Archive / Volume 9, Issue 30

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 (3736)

All Articles published online

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

Item

Count

PDF

285

WORD

HTML

2136

Figures (1-2)

193

Tables (1-1)

176

Sum=2878

Publishing Process of This Article

The chart showing Browse series, Download series.

Item

Count

Browse

251

Download

607

Sum=858

Oct 26, 2021 (publication date) through Jul 24, 2024

Times Cited of This Article

Times Cited (1)

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. Oct 26, 2021; 9(30): 9302-9309
Published online Oct 26, 2021. doi: 10.12998/wjcc.v9.i30.9302

Full Size Figure Download Figure

Figure 1 Clinical phenotypic characteristics of the proband. A: Adducted thumbs, symmetrical limbs, and permanently stretched limbs; B: No obvious gaze and high hairline; C and D: High arch feet.

Citation: Ding FJ, Lyu GZ, Zhang VW, Jin H. Missense mutation in DYNC1H1 gene caused psychomotor developmental delay and muscle weakness: A case report. World J Clin Cases 2021; 9(30): 9302-9309
URL: https://www.wjgnet.com/2307-8960/full/v9/i30/9302.htm
DOI: https://dx.doi.org/10.12998/wjcc.v9.i30.9302