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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Veröffentlicht in:Meta Gene
Hauptverfasser: 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: Artigo
Sprache:Inglês
Veröffentlicht: Elsevier 2014
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Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4287858/
https://ncbi.nlm.nih.gov/pubmed/25606422
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mgene.2014.04.008
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