Novel GRN Mutations in Patients with Corticobasal Syndrome

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Rare Neurodegenerative Diseases: Clinical and Genetic Update.Corticobasal degeneration: key emerging issues.

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Novel GRN Mutations in Patients with Corticobasal Syndrome

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http://www.wikidata.org/entity/Q36671072

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2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

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Novel GRN Mutations in Patients with Corticobasal Syndrome

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Novel GRN Mutations in Patients with Corticobasal Syndrome

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Item

label

Novel GRN Mutations in Patients with Corticobasal Syndrome

@ast

Novel GRN Mutations in Patients with Corticobasal Syndrome

@en

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Novel GRN Mutations in Patients with Corticobasal Syndrome

@ast

Novel GRN Mutations in Patients with Corticobasal Syndrome

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P1476

Novel GRN Mutations in Patients with Corticobasal Syndrome

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P2093

Christine Sato

http://www.w3.org/2001/XMLSchema#string

Danielle Moreno

http://www.w3.org/2001/XMLSchema#string

Ekaterina Rogaeva

http://www.w3.org/2001/XMLSchema#string

Maria Carmela Tartaglia

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P2860

Progranulin in frontotemporal lobar degeneration and neuroinflammation

C9orf72 repeat expansions are a rare genetic cause of parkinsonism

Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia

Impulsivity, frontal lobes and risk for addiction

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration.

Autosomal dominant frontotemporal lobar degeneration due to the C9ORF72 hexanucleotide repeat expansion: late-onset psychotic clinical presentation.

Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome): report of the NINDS-SPSP international workshop.

Corticobasal degeneration and its relationship to progressive supranuclear palsy and frontotemporal dementia.

A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series

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srep22913

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22913

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scholarly article

P356

10.1038/SREP22913

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P407

English

P478

http://www.w3.org/2001/XMLSchema#string

P50

Mahdi Ghani

Foad Taghdiri

P577

2016-03-10T00:00:00Z

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297753224

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26961809

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P932

4785496

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Novel GRN Mutations in Patients with Corticobasal Syndrome

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P2860

P2860

Novel GRN Mutations in Patients with Corticobasal Syndrome

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P407

P478

P50

P577

P5875

P698

P932

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P407

P478

P50

P577

P5875

P698

P932