Frontotemporal dementia: from Mendelian genetics towards genome wide association studies. - Wikidata - awgldk - TriplyDB

Frontotemporal dementia: from Mendelian genetics towards genome wide association studies.

Frontotemporal dementia: from Mendelian genetics towards genome wide association studies.

http://www.wikidata.org/entity/Q37928504

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Genome-wide association studies in neurology.A novel MAPT mutation, G55R, in a frontotemporal dementia patient leads to altered Tau function.FUS and TDP43 genetic variability in FTD and CBS A novel Alzheimer disease locus located near the gene encoding tau protein.Pathways to neurodegeneration: mechanistic insights from GWAS in Alzheimer's disease, Parkinson's disease, and related disorders Schizophrenia and frontotemporal dementia: shared causation?Genetics and underlying pathology of dementia.Proteomics as an innovative tool to investigate frontotemporal disorders.Genetics of Frontotemporal Lobar Degeneration: From the Bench to the Clinic.Frontotemporal dementia parkinsonism: Clinical findings in a large Iranian family.Next frontiers in the genetic epidemiology of Alzheimer's disease Chronic traumatic encephalopathy-integration of canonical traumatic brain injury secondary injury mechanisms with tau pathology.Dementia: a new algorithm for molecular diagnostics in FTLD.

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P2860

Frontotemporal dementia: from Mendelian genetics towards genome wide association studies.

http://www.wikidata.org/entity/Q37928504

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artigo científico

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Frontotemporal dementia: from Mendelian genetics towards genome wide association studies.

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Frontotemporal dementia: from Mendelian genetics towards genome wide association studies.

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type

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Frontotemporal dementia: from Mendelian genetics towards genome wide association studies.

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Frontotemporal dementia: from Mendelian genetics towards genome wide association studies.

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prefLabel

Frontotemporal dementia: from Mendelian genetics towards genome wide association studies.

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Frontotemporal dementia: from Mendelian genetics towards genome wide association studies.

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S12031-011-9635-Y

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Journal of Molecular Neuroscience

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Frontotemporal dementia: from Mendelian genetics towards genome wide association studies.

@en

P2860

Analysis of IFT74 as a candidate gene for chromosome 9p-linked ALS-FTD

ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B)

Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia

Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

A map of human genome variation from population-scale sequencing

Functional MAPT haplotypes: bridging the gap between genotype and neuropathology

A second generation human haplotype map of over 3.1 million SNPs

Evolutionary toggling of the MAPT 17q21.31 inversion region

A haplotype map of the human genome

P2888

s12031-011-9635-y

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500-515

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scholarly article

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10.1007/S12031-011-9635-Y

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3

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Raffaele Ferrari

John Anthony Hardy

Parastoo Momeni

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2011-09-06T00:00:00Z

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genome-wide association study