Keratin 13 mutations associated with oral white sponge nevus in two Chinese families

Keratin 13 mutations associated with oral white sponge nevus in two Chinese families

White sponge nevus (WSN) is an autosomal dominant hereditary disease. Keratin 4 (KRT4) and Keratin 13 (KRT13) gene mutations were involved in the WSN. We recruited two WSN Chinese families, and oral lesion biopsy with hematoxylin and eosin staining showed that patients had significant pathological c...

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Bibliographic Details
Main Authors: Cai, Wenping, Chen, Zhenghu, Jiang, Beizhan, Yu, Fang, Xu, Ping, Wang, Mu, Wan, Rui, Liu, Junjun, Xue, Zhigang, Yang, Jianhua, Liu, Shangfeng, Wang, Xiaoping
Format: Online
Language:English
Published: Elsevier 2014
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4287858/

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https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4287858/

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