Mutation p.R156H of KRT10 responsible for severe phenotype...

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Therapeutics and Clinical Risk Management 2014 / 09

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

Zhiliang,, Liu, Qiao, wang, hongsheng, Wang, Aimin, Li, Chengrang
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Language:
english
Journal:
Therapeutics and Clinical Risk Management
DOI:
10.2147/tcrm.s69128
Date:
September, 2014
File:
PDF, 825 KB
english, 2014
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