The G389R mutation in the MAPT gene presenting as sporadic corticobasal syndrome.

The G389R mutation in the MAPT gene presenting as sporadic corticobasal syndrome.

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http://www.wikidata.org/entity/Q42525223
Frontotemporal lobar degeneration: old knowledge and new insight into the pathogenetic mechanisms of tau mutationsInvited review: Frontotemporal dementia caused by microtubule-associated protein tau gene (MAPT) mutations: a chameleon for neuropathology and neuroimagingCharacterization of Movement Disorder Phenomenology in Genetically Proven, Familial Frontotemporal Lobar Degeneration: A Systematic Review and Meta-Analysis.Exome sequencing in familial corticobasal degenerationAn algorithm for genetic testing of frontotemporal lobar degenerationA familial form of parkinsonism, dementia, and motor neuron disease: a longitudinal study.Corticobasal degeneration: a pathologically distinct 4R tauopathy.The multiple phenotypes of corticobasal syndrome and corticobasal degeneration: implications for further study."Atypical" atypical parkinsonism: new genetic conditions presenting with features of progressive supranuclear palsy, corticobasal degeneration, or multiple system atrophy-a diagnostic guide.Parkinsonism, movement disorders and genetics in frontotemporal dementia.The clinical spectrum of sporadic and familial forms of frontotemporal dementia.A progranulin mutation associated with cortico-basal syndrome in an Italian family expressing different phenotypes of fronto-temporal lobar degeneration.Intrafamilial variable phenotype including corticobasal syndrome in a family with p.P301L mutation in the MAPT gene: first report in South America.FTDP-17 with Pick body-like inclusions associated with a novel tau mutation, p.E372G.A Novel MAPT Mutation Causing Corticobasal Syndrome Led by Progressive Apraxia of Speech.
P2860

The G389R mutation in the MAPT gene presenting as sporadic corticobasal syndrome.

Item
http://www.wikidata.org/entity/Q42525223
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh
2008年學術文章
@zh-hant
name
The G389R mutation in the MAPT gene presenting as sporadic corticobasal syndrome.
@en
The G389R mutation in the MAPT gene presenting as sporadic corticobasal syndrome.
@nl
type
label
The G389R mutation in the MAPT gene presenting as sporadic corticobasal syndrome.
@en
The G389R mutation in the MAPT gene presenting as sporadic corticobasal syndrome.
@nl
prefLabel
The G389R mutation in the MAPT gene presenting as sporadic corticobasal syndrome.
@en
The G389R mutation in the MAPT gene presenting as sporadic corticobasal syndrome.
@nl
P1433
P1476
P2093
P2860
P304
P31
P356
P407
P433
P478
P50
P577
P698
P356
P1433
P1476
The G389R mutation in the MAPT gene presenting as sporadic corticobasal syndrome.
@en
P2093
P2860
P304
P31
P356
P407
P433
P478
P50
P577
P698