Different mutations at V363 MAPT codon are associated with atypical clinical phenotypes and show unusual structural and functional features.
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Frontotemporal lobar degeneration: old knowledge and new insight into the pathogenetic mechanisms of tau mutationsLinking traumatic brain injury to chronic traumatic encephalopathy: identification of potential mechanisms leading to neurofibrillary tangle developmentThe Role of MAPT in Neurodegenerative Diseases: Genetics, Mechanisms and TherapyA network of RNA and protein interactions in Fronto Temporal Dementia.Evaluating pathogenic dementia variants in posterior cortical atrophy.The clinical spectrum of sporadic and familial forms of frontotemporal dementia.Visual Dysfunction in Posterior Cortical Atrophy.Posterior cortical atrophy as a primary clinical phenotype of corticobasal syndrome with a progranulin gene rs5848 TT genotype.
P2860
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P2860
Different mutations at V363 MAPT codon are associated with atypical clinical phenotypes and show unusual structural and functional features.
description
2013 nî lūn-bûn
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2013年の論文
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2013年学术文章
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2013年学术文章
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2013年学术文章
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2013年学术文章
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2013年学术文章
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2013年学术文章
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2013年學術文章
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2013年學術文章
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name
Different mutations at V363 MA ...... tural and functional features.
@en
Different mutations at V363 MA ...... tural and functional features.
@nl
type
label
Different mutations at V363 MA ...... tural and functional features.
@en
Different mutations at V363 MA ...... tural and functional features.
@nl
prefLabel
Different mutations at V363 MA ...... tural and functional features.
@en
Different mutations at V363 MA ...... tural and functional features.
@nl
P2093
P50
P1476
Different mutations at V363 MA ...... ctural and functional features
@en
P2093
Antonio Bastone
Antonio Emanuele Elia
Claudia Morelli
Davide Pareyson
Elena Piccoli
Ettore Salsano
Francesca Del Sorbo
Giacomina Rossi
Giulia Mazzoleni
Laura Cantù
P304
P356
10.1016/J.NEUROBIOLAGING.2013.08.004
P50
P577
2013-09-07T00:00:00Z