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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Detalles Bibliográficos
Autores principales: Cai, Wenping, Chen, Zhenghu, Jiang, Beizhan, Yu, Fang, Xu, Ping, Wang, Mu, Wan, Rui, Liu, Junjun, Xue, Zhigang, Yang, Jianhua, Liu, Shangfeng, Wang, Xiaoping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4287858/
https://www.ncbi.nlm.nih.gov/pubmed/25606422
http://dx.doi.org/10.1016/j.mgene.2014.04.008

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4287858/
https://www.ncbi.nlm.nih.gov/pubmed/25606422
http://dx.doi.org/10.1016/j.mgene.2014.04.008

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