MutL homolog 1 germline mutation c.(453+1_454-1)_(545+1_546-1)del identified in lynch syndrome: A case report and review of literature

doi:10.12998/wjcc.v10.i20.7105

Advanced Search

BPG is committed to discovery and dissemination of knowledge

Home / Archive / Volume 10, Issue 20

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 (2674)

All Articles published online

The chart showing PDF series, WORD series, HTML series, Figures (1-4) series, Tables (1-3) series.

Item

Count

PDF

180

WORD

HTML

1248

Figures (1-4)

371

Tables (1-3)

135

Sum=1998

Publishing Process of This Article

The chart showing Browse series, Download series.

Item

Count

Browse

201

Download

475

Sum=676

Jul 16, 2022 (publication date) through May 13, 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. Jul 16, 2022; 10(20): 7105-7115
Published online Jul 16, 2022. doi: 10.12998/wjcc.v10.i20.7105

Full Size Figure Download Figure

Figure 3 Figures related to gene test results. A deletion mutation of exon 6 was found in the MLH1 gene.

Citation: Zhang XW, Jia ZH, Zhao LP, Wu YS, Cui MH, Jia Y, Xu TM. MutL homolog 1 germline mutation c.(453+1_454-1)_(545+1_546-1)del identified in lynch syndrome: A case report and review of literature. World J Clin Cases 2022; 10(20): 7105-7115
URL: https://www.wjgnet.com/2307-8960/full/v10/i20/7105.htm
DOI: https://dx.doi.org/10.12998/wjcc.v10.i20.7105