Familial Lund frontotemporal dementia caused by C9ORF72 hexanucleotide expansion.

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Phenotypic Heterogeneity of Monogenic Frontotemporal Dementia The clinical spectrum of sporadic and familial forms of frontotemporal dementia.Frontotemporal dementia with a C9ORF72 expansion in a Swedish family: clinical and neuropathological characteristics.

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Familial Lund frontotemporal dementia caused by C9ORF72 hexanucleotide expansion.

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http://www.wikidata.org/entity/Q36035170

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2012 nî lūn-bûn

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

@zh-hk

2012年論文

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2012年論文

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2012年论文

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2012年论文

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2012年论文

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Familial Lund frontotemporal dementia caused by C9ORF72 hexanucleotide expansion.

@ast

Familial Lund frontotemporal dementia caused by C9ORF72 hexanucleotide expansion.

@en

type

Item

label

Familial Lund frontotemporal dementia caused by C9ORF72 hexanucleotide expansion.

@ast

Familial Lund frontotemporal dementia caused by C9ORF72 hexanucleotide expansion.

@en

prefLabel

Familial Lund frontotemporal dementia caused by C9ORF72 hexanucleotide expansion.

@ast

Familial Lund frontotemporal dementia caused by C9ORF72 hexanucleotide expansion.

@en

P1476

Familial Lund frontotemporal dementia caused by C9ORF72 hexanucleotide expansion.

@en

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Bryan J Traynor

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Elisa Majounie

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

Lars Gustafson

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Ulla Passant

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Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia

Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study

A harmonized classification system for FTLD-TDP pathology

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

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions.

Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.

Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study.

Chromosome 9 ALS and FTD locus is probably derived from a single founder

Familial frontotemporal dementia with amyotrophic lateral sclerosis and a shared haplotype on chromosome 9p.

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1850.e13-6

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scholarly article

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10.1016/J.NEUROBIOLAGING.2012.02.019

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2012-04-06T00:00:00Z

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22483864

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4562220

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Familial Lund frontotemporal dementia caused by C9ORF72 hexanucleotide expansion.

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P2860

P2860

Familial Lund frontotemporal dementia caused by C9ORF72 hexanucleotide expansion.

description

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type

label

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P932