Perry syndrome with progressive supranuclear palsy-like phenotype in a Portuguese family Long-term clinical follow-up

被引：6

作者：

Barreto, Rui Duarte ^{[1
]}

Rodrigues, Rita ^{[2
]}

Roriz, Jose Mario ^{[2
]}

Alonso, Isabel ^{[3
,4
]}

Magalhaes, Marina ^{[5
]}

机构：

[1] Ctr Hosp Univ Lisboa Norte, Neurol Dept, Lisbon, Portugal

[2] Ctr Hosp Entre Douro E Vouga, Neurol Dept, Rua Dr Candido de Pinho, P-4520211 Santa Maria Feira, Portugal

[3] Univ Porto, Inst Invest & Inovacao Saude I3S, IBMC Inst Mol & Cell Biol, UnIGENe, Porto, Portugal

[4] Genetyca ICM, Porto, Portugal

[5] Ctr Hosp Univ Porto, Neurol Dept, Porto, Portugal

来源：

PARKINSONISM & RELATED DISORDERS | 2021年 / 84卷

关键词：

DCTN1; MUTATION; PARKINSONISM;

D O I：

10.1016/j.parkreldis.2021.02.004

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：74 / 76

页数：3

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