Current understanding of human genetics and genetic analysis of psoriasis
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Title
Current understanding of human genetics and genetic analysis of psoriasis
Authors
Keywords
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Journal
JOURNAL OF DERMATOLOGY
Volume 39, Issue 3, Pages 231-241
Publisher
Wiley
Online
2012-02-22
DOI
10.1111/j.1346-8138.2012.01504.x
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- (2010) Kai Wang et al. AMERICAN JOURNAL OF HUMAN GENETICS
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