Review and update on the molecular basis of Leber congenital amaurosis

doi:10.12998/wjcc.v3.i2.112

Advanced Search

BPG is committed to discovery and dissemination of knowledge

Home / Archive / Volume 3, Issue 2

This Article

Academic Content and Language Evaluation 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 (16025)

All Articles published online

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

Item

Count

PDF

939

WORD

477

HTML

10060

Figures (1-3)

385

Tables (1-1)

249

Sum=12110

Featured Article

The chart showing Browse series, Download series.

Item

Count

Browse

564

Download

1071

Sum=1635

Publishing Process of This Article

Item

Count

Browse

1086

Download

1194

Sum=2280

Feb 16, 2015 (publication date) through Nov 5, 2024

Times Cited of This Article

Times Cited (95)

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

Review

World J Clin Cases. Feb 16, 2015; 3(2): 112-124
Published online Feb 16, 2015. doi: 10.12998/wjcc.v3.i2.112

Open in New Tab Full Size Figure Download Figure

Figure 1 Patient´s fundus with RPE65 mutations.

Open in New Tab Full Size Figure Download Figure

Figure 2 Patient´s fundus with CRB1 mutations.

Open in New Tab Full Size Figure Download Figure

Figure 3 Patient´s fundus with RDH12 mutations.

Citation: Chacon-Camacho OF, Zenteno JC. Review and update on the molecular basis of Leber congenital amaurosis. World J Clin Cases 2015; 3(2): 112-124
URL: https://www.wjgnet.com/2307-8960/full/v3/i2/112.htm
DOI: https://dx.doi.org/10.12998/wjcc.v3.i2.112