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Common FLG Mutation K4671X Not Associated with Atopic Dermatitis in Han Chinese in a Family Association Study

Overview of attention for article published in PLOS ONE, November 2012
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Title
Common FLG Mutation K4671X Not Associated with Atopic Dermatitis in Han Chinese in a Family Association Study
Published in
PLOS ONE, November 2012
DOI 10.1371/journal.pone.0049158
Pubmed ID
Authors

Ruhong Cheng, Ming Li, Hui Zhang, Yifeng Guo, Xilan Chen, Jianfeng Tao, Aifang Jiang, Jiecheng Gan, Huaishan Qi, Hong Yu, Wanqing Liao, Zhirong Yao

Abstract

Filaggrin gene (FLG) mutations have been identified as the cause of ichthyosis vulgaris (IV) and major predisposing factors for atopic dermatitis (AD). The relationship among AD, IV and FLG mutations has not been clarified yet. Mutations 3321delA and K4671X, two of the most common mutations in Chinese patients, were both statistically associated with AD in case-control studies.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 20 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 20 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 5 25%
Researcher 3 15%
Student > Doctoral Student 1 5%
Student > Bachelor 1 5%
Student > Ph. D. Student 1 5%
Other 3 15%
Unknown 6 30%
Readers by discipline Count As %
Agricultural and Biological Sciences 3 15%
Medicine and Dentistry 2 10%
Neuroscience 2 10%
Immunology and Microbiology 2 10%
Mathematics 1 5%
Other 3 15%
Unknown 7 35%