Alpha-synuclein pathology and Parkinsonism associated with POLG1 mutations and multiple mitochondrial DNA deletions

被引：39
|
作者：
Betts-Henderson, J. [1 ]
Jaros, E. [2 ,3 ]
Krishnan, K. J. [1 ]
Perry, R. H. [2 ,3 ]
Reeve, A. K. [1 ]
Schaefer, A. M. [1 ]
Taylor, R. W. [1 ]
Turnbull, D. M. [1 ]
机构：
[1] Univ Newcastle, Mitochondrial Res Grp, Newcastle Upon Tyne, Tyne & Wear, England
[2] Univ Newcastle, Inst Ageing & Hlth, Newcastle Upon Tyne, Tyne & Wear, England
[3] Newcastle Upon Tyne Hosp NHS Trust, Div Neuropathol, Newcastle Upon Tyne, Tyne & Wear, England
来源：
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY | 2009年 / 35卷 / 01期
基金：
英国惠康基金; 英国医学研究理事会;
关键词：
SUBSTANTIA-NIGRA NEURONS; POLYMERASE-GAMMA; DISEASE; DEMENTIA;
D O I：
10.1111/j.1365-2990.2008.00981.x
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
[No abstract available]
引用
收藏
页码：120 / 124
页数：5
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