文献
J-GLOBAL ID:201102222268214634
整理番号:11A1812940
LRRK2遺伝子の包括的変異解析は常染色体優性Parkinson病との関連を支持する変異体を顕わす
Comprehensive mutational analysis of LRRK2 reveals variants supporting association with autosomal dominant Parkinson’s disease
著者 (13件):
SEKI Naomi
(Univ. Tokyo, Tokyo, JPN)
,
TAKAHASHI Yuji
(Univ. Tokyo, Tokyo, JPN)
,
TOMIYAMA Hiroyuki
(Juntendo Univ. School of Medicine, Tokyo, JPN)
,
ROGAEVA Ekaterina
(Univ. Toronto, Ontario, CAN)
,
MURAYAMA Shigeo
(Tokyo Metropolitan Inst. Gerontology, Tokyo, JPN)
,
MIZUNO Yoshikuni
(Juntendo Univ. School of Medicine, Tokyo, JPN)
,
HATTORI Nobutaka
(Juntendo Univ. School of Medicine, Tokyo, JPN)
,
MARRAS Connie
(Toronto Western Hospital, Ontario, CAN)
,
LANG Anthony E
(Toronto Western Hospital, Ontario, CAN)
,
ST GEORGE-HYSLOP Peter
(Univ. Toronto, Ontario, CAN)
,
ST GEORGE-HYSLOP Peter
(Univ. Cambridge, Cambridge, GBR)
,
GOTO Jun
(Univ. Tokyo, Tokyo, JPN)
,
TSUJI Shoji
(Univ. Tokyo, Tokyo, JPN)
資料名:
Journal of Human Genetics
(Journal of Human Genetics)
巻:
56
号:
9
ページ:
671-675
発行年:
2011年09月
JST資料番号:
Z0756A
ISSN:
1434-5161
資料種別:
逐次刊行物 (A)
記事区分:
原著論文
発行国:
イギリス (GBR)
言語:
英語 (EN)