FASGene Copy Numbers are Associated with Susceptibility to Behçet Disease and VKH Syndrome in Han Chinese-Reference-Cited by-全球学者库

FASGene Copy Numbers are Associated with Susceptibility to Behçet Disease and VKH Syndrome in Han Chinese

Published:2015-08-03 Issue:11 Volume:36 Page:1064-1069
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Yu Hongsong¹,Luo Le¹,Wu Lili¹,Zheng Minming¹,Zhang Lijun¹,Liu Yunjia¹,Li Hua¹,Cao Qingfeng¹,Kijlstra Aize²,Yang Peizeng¹

Affiliation:

1. The First Affiliated Hospital of Chongqing Medical University, Chongqing Key Laboratory of Ophthalmology and Chongqing Eye Institute; Chongqing P. R. China

2. University Eye Clinic Maastricht; Maastricht The Netherlands

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.22829/fullpdf

Reference44 articles.

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3. Correlating multiallelic copy number polymorphisms with disease susceptibility;Cantsilieris;Hum Mutat,2013

4. Association of FCGR3A and FCGR3B Copy number variations with systemic lupus erythematosus and rheumatoid arthritis in Taiwanese patients;Chen;Arthritis Rheum,2014

5. Quantitation of Fas and Fas ligand gene expression in human ovarian, cervical and endometrial carcinomas using real-time quantitative RT-PCR;Das;Br J Cancer,2000

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