Alzheimer disease-like clinical phenotype in a family with FTDP-17 caused by a MAPT R406W mutation

✍ Scribed by S. G. Lindquist; I. E. Holm; M. Schwartz; I. Law; J. Stokholm; M. Batbayli; G. Waldemar; J. E. Nielsen

• Book ID: 111065424
• Publisher: John Wiley and Sons
• Year: 2008
• Tongue: English
• Weight: 778 KB
• Volume: 15
• Category: Article
• ISSN: 1351-5101
• DOI: 10.1111/j.1468-1331.2008.02069.x