Mutation p.R156H of KRT10 responsible for severe phenotype of epidermolytic ichthyosis in a Chinese family

Detalles Bibliográficos
Autores principales: Li, Zhiliang, Liu, Qiao, Wang, Aimin, Wang, Hongsheng, Li, Chengrang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Letter
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4159368/
https://www.ncbi.nlm.nih.gov/pubmed/25214791
http://dx.doi.org/10.2147/TCRM.S69128
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author Li, Zhiliang
Liu, Qiao
Wang, Aimin
Wang, Hongsheng
Li, Chengrang
author_facet Li, Zhiliang
Liu, Qiao
Wang, Aimin
Wang, Hongsheng
Li, Chengrang
author_sort Li, Zhiliang
collection PubMed
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spelling pubmed-41593682014-09-11 Mutation p.R156H of KRT10 responsible for severe phenotype of epidermolytic ichthyosis in a Chinese family Li, Zhiliang Liu, Qiao Wang, Aimin Wang, Hongsheng Li, Chengrang Ther Clin Risk Manag Letter Dove Medical Press 2014-09-01 /pmc/articles/PMC4159368/ /pubmed/25214791 http://dx.doi.org/10.2147/TCRM.S69128 Text en © 2014 Li et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Letter
Li, Zhiliang
Liu, Qiao
Wang, Aimin
Wang, Hongsheng
Li, Chengrang
Mutation p.R156H of KRT10 responsible for severe phenotype of epidermolytic ichthyosis in a Chinese family
title Mutation p.R156H of KRT10 responsible for severe phenotype of epidermolytic ichthyosis in a Chinese family
title_full Mutation p.R156H of KRT10 responsible for severe phenotype of epidermolytic ichthyosis in a Chinese family
title_fullStr Mutation p.R156H of KRT10 responsible for severe phenotype of epidermolytic ichthyosis in a Chinese family
title_full_unstemmed Mutation p.R156H of KRT10 responsible for severe phenotype of epidermolytic ichthyosis in a Chinese family
title_short Mutation p.R156H of KRT10 responsible for severe phenotype of epidermolytic ichthyosis in a Chinese family
title_sort mutation p.r156h of krt10 responsible for severe phenotype of epidermolytic ichthyosis in a chinese family
topic Letter
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4159368/
https://www.ncbi.nlm.nih.gov/pubmed/25214791
http://dx.doi.org/10.2147/TCRM.S69128
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