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Letter - Clinical
Autosomal dominant monilethrix with incomplete penetrance due to a novel KRT86 mutation in a Chinese family
Ru Dai, Tingting Wang, Xianjie Wu
Corresponding author
wuxianjie@zju.edu.cn

Corresponding author.
Department of Dermatology, Zhejiang University School of Medicine Second Affiliated Hospital, Hangzhou, Zhejiang, China
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ISSN: 03650596
Original language: English
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