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

标题
Alzheimer disease-like clinical phenotype in a family with FTDP-17 caused by a MAPT R406W mutation
作者
关键词
-
出版物
EUROPEAN JOURNAL OF NEUROLOGY
Volume 15, Issue 4, Pages 377-385
出版商
Wiley
发表日期
2008-02-18
DOI
10.1111/j.1468-1331.2008.02069.x

向作者/读者发起求助以获取更多资源

Find the ideal target journal for your manuscript

Explore over 38,000 international journals covering a vast array of academic fields.

Search

Ask a Question. Answer a Question.

Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.

Get Started