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

页码：120 / 124

页数：5

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