A novel KRT5 mutation, p.Lys199Asn, is associated with three subtypes of epidermolysis bullosa simplex phenotypes in a single Chinese family

✍ Scribed by Deng, Weiping; Yuan, Ping; Lai, Wei; Chen, Minhua; Wang, Yiming; Dai, Shaoxia

• Book ID: 119293783
• Publisher: Elsevier Science
• Year: 2011
• Tongue: English
• Weight: 318 KB
• Volume: 64
• Category: Article
• ISSN: 0923-1811
• DOI: 10.1016/j.jdermsci.2011.09.003