Sensory and motor neuronopathy in a patient with the A382P TDP-43 mutation.

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Genetic overlap between apparently sporadic motor neuron diseases.Extra-motor abnormalities in amyotrophic lateral sclerosis: another layer of heterogeneity.

P2860

Q34479235-39670E62-0578-4B5B-9DC9-718A44A98DAA Q39041271-EE3A80E4-15CB-4105-B38E-43A94F3F7FDB

P2860

Sensory and motor neuronopathy in a patient with the A382P TDP-43 mutation.

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http://www.wikidata.org/entity/Q41885438

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2011 nî lūn-bûn

@nan

2011年の論文

@ja

2011年論文

@yue

2011年論文

@zh-hant

2011年論文

@zh-hk

2011年論文

@zh-mo

2011年論文

@zh-tw

2011年论文

@wuu

2011年论文

@zh

2011年论文

@zh-cn

name

Sensory and motor neuronopathy in a patient with the A382P TDP-43 mutation.

@en

type

Item

label

Sensory and motor neuronopathy in a patient with the A382P TDP-43 mutation.

@en

prefLabel

Sensory and motor neuronopathy in a patient with the A382P TDP-43 mutation.

@en

P1476

Sensory and motor neuronopathy in a patient with the A382P TDP-43 mutation.

@en

P2093

Guillemette Jousserand

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Jean-Christophe Antoine

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

Jean-Philippe Camdessanché

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

Véronique V Belzil

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

P2860

Predicting deleterious amino acid substitutions

A method and server for predicting damaging missense mutations

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

TDP-43 localizes in mRNA transcription and processing sites in mammalian neurons

TARDBP 3'-UTR variant in autopsy-confirmed frontotemporal lobar degeneration with TDP-43 proteinopathy

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration

Transgenic rat model of neurodegeneration caused by mutation in the TDP gene.

TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis

Phosphorylation of S409/410 of TDP-43 is a consistent feature in all sporadic and familial forms of TDP-43 proteinopathies

P2888

1750-1172-6-4

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scholarly article

P356

10.1186/1750-1172-6-4

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P478

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P50

Guy A. Rouleau

Philippe Convers

Christelle Créac'h

P577

2011-02-05T00:00:00Z

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49811240

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P6179

1002007923

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21294910

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P932

3042904

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Sensory and motor neuronopathy in a patient with the A382P TDP-43 mutation.

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P2860

P2860

Sensory and motor neuronopathy in a patient with the A382P TDP-43 mutation.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P478

P50

P577

P5875

P6179

P698

P932

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P478

P50

P577

P5875

P6179

P698

P932