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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Detalhes bibliográficos
Publicado no:Meta Gene
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
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2014
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Article
Acesso em linha: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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