An Indian child with Kindler syndrome resulting from a new homozygous nonsense mutation (C468X) in the KIND1 gene

✍ Scribed by G. Sethuraman; H. Fassihi; G. H. S. Ashton; A. Bansal; M. Kabra; V. K. Sharma; J. A. McGrath

• Book ID: 108693298
• Publisher: John Wiley and Sons
• Year: 2005
• Tongue: English
• Weight: 243 KB
• Volume: 30
• Category: Article
• ISSN: 0307-6938
• DOI: 10.1111/j.1365-2230.2004.01712.x