Parkinsonism and distinct dementia patterns in a family with the MAPT R406W mutation. - Wikidata - awgldk - TriplyDB

Parkinsonism and distinct dementia patterns in a family with the MAPT R406W mutation.

Parkinsonism and distinct dementia patterns in a family with the MAPT R406W mutation.

http://www.wikidata.org/entity/Q37146802

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Parkinsonian syndrome in familial frontotemporal dementia Characterization of Movement Disorder Phenomenology in Genetically Proven, Familial Frontotemporal Lobar Degeneration: A Systematic Review and Meta-Analysis.Evaluating pathogenic dementia variants in posterior cortical atrophy.Young-onset frontotemporal dementia in a homozygous tau R406W mutation carrier Early-Onset Alzheimer Disease and Candidate Risk Genes Involved in Endolysosomal Transport.The Genetics of Monogenic Frontotemporal Dementia.Exome Sequencing of Extended Families with Alzheimer's Disease Identifies Novel Genes Implicated in Cell Immunity and Neuronal Function.Slowly progressive dementia caused by MAPT R406W mutations: longitudinal report on a new kindred and systematic review.Slowly progressive behavioural presentation in two UK cases with the R406W MAPT mutation.

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Parkinsonism and distinct dementia patterns in a family with the MAPT R406W mutation.

http://www.wikidata.org/entity/Q37146802

description

article científic

@ca

article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 30 May 2013

@en

vedecký článok

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vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Parkinsonism and distinct dementia patterns in a family with the MAPT R406W mutation.

@en

Parkinsonism and distinct dementia patterns in a family with the MAPT R406W mutation.

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type

label

Parkinsonism and distinct dementia patterns in a family with the MAPT R406W mutation.

@en

Parkinsonism and distinct dementia patterns in a family with the MAPT R406W mutation.

@nl

prefLabel

Parkinsonism and distinct dementia patterns in a family with the MAPT R406W mutation.

@en

Parkinsonism and distinct dementia patterns in a family with the MAPT R406W mutation.

@nl

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P356

J.JALZ.2013.02.011

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Alzheimer's and Dementia

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Parkinsonism and distinct dementia patterns in a family with the MAPT R406W mutation.

@en

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Adam C Naj

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Brian W Kunkle

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John R Gilbert

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Martin A Kohli

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Regina M Carney

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Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease

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Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease

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360-365

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10.1016/J.JALZ.2013.02.011

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3

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10

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Margaret A. Pericak-Vance

Stephan Züchner

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2013-05-30T00:00:00Z

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23727082

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Parkinson's disease

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3762928

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