A Huntington's disease phenocopy characterized by pallido-nigro-luysian degeneration with brain iron accumulation and p62-positive glial inclusions

被引：12

作者：

Ahmed, Z. ^{[1
]}

Tabrizi, S. J. ^{[2
]}

Li, A. ^{[1
]}

Houlden, H. ^{[1
]}

Sailer, A. ^{[1
]}

Lees, A. J. ^{[1
]}

Revesz, T. ^{[1
]}

Holton, J. L. ^{[1
]}

机构：

[1] Queen Sq Brain Bank, Dept Mol Neurosci, London, England

[2] UCL Inst Neurol, MRC Prion Unit, London, England

来源：

NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY | 2010年 / 36卷 / 06期

基金：

英国医学研究理事会;

关键词：

MULTIPLE SYSTEM ATROPHY; NEURODEGENERATIVE DISEASE; CYTOPLASMIC INCLUSIONS; ALPHA-SYNUCLEIN; GENE; PARKINSONISM; DIAGNOSIS; PATHOLOGY; MUTATION;

D O I：

10.1111/j.1365-2990.2010.01093.x

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

100204 [神经病学];

摘要：

[No abstract available]

引用

页码：551 / 557

页数：7

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