CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study-Reference-Cited by-同舟云学术

CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study

Published:2015-03 Issue:3 Volume:14 Page:274-282
ISSN:1474-4422
Container-title:The Lancet Neurology
language:en
Short-container-title:The Lancet Neurology

Author:

Funayama Manabu,Ohe Kenji,Amo Taku,Furuya Norihiko,Yamaguchi Junji,Saiki Shinji,Li Yuanzhe,Ogaki Kotaro,Ando Maya,Yoshino Hiroyo,Tomiyama Hiroyuki,Nishioka Kenya,Hasegawa Kazuko,Saiki Hidemoto,Satake Wataru,Mogushi Kaoru,Sasaki Ryogen,Kokubo Yasumasa,Kuzuhara Shigeki,Toda Tatsushi,Mizuno Yoshikuni,Uchiyama Yasuo,Ohno Kinji,Hattori Nobutaka

Funder

Scientific Research on Innovative Areas

Young Scientists

Grant-in-Aid for Challenging Exploratory Research

Grant-in-Aid for Scientific Research from the Japan Society for the Promotion of Science

Publisher

Elsevier BV

Subject

Clinical Neurology

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2. The genetics of Parkinson's disease: progress and therapeutic implications;Singleton;Mov Disord,2013