A novel point mutation of keratin 17 (KRT17) in a Japanese family with pachyonychia congenita type 2: an RNA-based genetic analysis using a single hair bulb

✍ Scribed by T. Tsuda; C. Ishikawa; N. Nakagawa; H. Konishi; M. Tarutani; M. Matsuki; K. Yamanishi

• Book ID: 108670152
• Publisher: John Wiley and Sons
• Year: 2008
• Tongue: English
• Weight: 173 KB
• Volume: 159
• Category: Article
• ISSN: 0007-0963
• DOI: 10.1111/j.1365-2133.2008.08684.x