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Analyses of the MAPT, PGRN, and C9orf72 mutations in Japanese patients with FTLD, PSP, and CBS

✍ Scribed by Kotaro Ogaki; Yuanzhe Li; Masashi Takanashi; Kei-Ichi Ishikawa; Tomonori Kobayashi; Takashi Nonaka; Masato Hasegawa; Masahiko Kishi; Hiroyo Yoshino; Manabu Funayama; Tetsuro Tsukamoto; Keiichi Shioya; Masayuki Yokochi; Hisamasa Imai; Ryogen Sasaki; Yasumasa Kokubo; Shigeki Kuzuhara; Yumiko Motoi; Hiroyuki Tomiyama; Nobutaka Hattori


Book ID
118064473
Publisher
Elsevier Science
Year
2013
Tongue
English
Weight
353 KB
Volume
19
Category
Article
ISSN
1353-8020

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