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February 7, 2019Clinical and Experimental Dermatology19 citations

Clinical and genetic features of Chinese patients with lichen and macular primary localized cutaneous amyloidosis

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PLPing LüEducation Department of Fujian ProvinceFWFangyao WuNanfang HospitalZRZhili RongShanghai Children's Medical Center

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Abstract

The present data indicate OSMR mutations as not only the main cause of fPLCA, but also the potential source of the pathogenesis of sPLCA, although the exact molecular mechanism remains unknown.

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Cite This Study

Lü et al. (2019) studied this question.

synapsesocial.com/papers/69d959ab9a6164e50fa3ca14https://doi.org/10.1111/ced.13925
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