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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Detaylı Bibliyografya
Yayımlandı:Meta Gene
Asıl Yazarlar: Cai, Wenping, Chen, Zhenghu, Jiang, Beizhan, Yu, Fang, Xu, Ping, Wang, Mu, Wan, Rui, Liu, Junjun, Xue, Zhigang, Yang, Jianhua, Liu, Shangfeng, Wang, Xiaoping
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Elsevier 2014
Konular:
Article
Online Erişim: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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