The lrrk2 p.Gly2019Ser mutation is uncommon in a Danish cohort with various neurodegenerative disorders

被引：3

作者：

Bech, Sara ^{[1
,2
]}

Norremolle, Anne ^{[1
]}

Winge, Kristian ^{[2
]}

Hasholt, Lis ^{[1
]}

Tommerup, Niels ^{[3
]}

Svenstrup, Kirsten ^{[1
,4
]}

Nielsen, Jorgen E. ^{[1
,4
]}

Hjermind, Lena E. ^{[1
,4
]}

机构：

[1] Univ Copenhagen, Panum Inst, Dept Cellular & Mol Med, Neurogenet Sect, DK-2200 Copenhagen, Denmark

[2] Bispebjerg Hosp, Dept Neurol, DK-2400 Copenhagen, Denmark

[3] Univ Copenhagen, Panum Inst, Dept Cellular & Mol Med, Wilhelm Johannsen Ctr Funct Genome Res, DK-2200 Copenhagen, Denmark

[4] Copenhagen Univ Hosp, Dept Neurol, Memory Disorders Res Grp, Neurogenet Clin, Copenhagen, Denmark

来源：

PARKINSONISM & RELATED DISORDERS | 2011年 / 17卷 / 05期

关键词：

LRRK2; PARK8; p.Gly2019Ser; Parkinsonism; Atypical parkinsonian syndromes;

D O I：

10.1016/j.parkreldis.2011.01.016

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

引用

页码：398 / 399

页数：2

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