P3-280: Alzheimer's disease-like clinical phenotype in a family with FTDP-17 caused by a MAPT R406W mutation

✍ Scribed by Lindquist, Suzanne G.; Holm, Ida E.; Schwartz, Marianne; Law, Ian; Stokholm, Jette; Batbayli, Mustafa; Waldemar, Gunhild; Nielsen, Jørgen E.

• Book ID: 122390223
• Publisher: Elsevier Science
• Year: 2008
• Tongue: English
• Weight: 58 KB
• Volume: 4
• Category: Article
• ISSN: 1552-5260
• DOI: 10.1016/j.jalz.2008.05.1848