ANXA11 mutations prevail in Chinese ALS patients with and without cognitive dementia.

about

ANXA11 mutations prevail in Chinese ALS patients with and without cognitive dementia.

Item

http://www.wikidata.org/entity/Q55002878

description

2018 nî lūn-bûn

@nan

2018年の論文

@ja

2018年学术文章

@wuu

2018年学术文章

@zh-cn

2018年学术文章

@zh-hans

2018年学术文章

@zh-my

2018年学术文章

@zh-sg

2018年學術文章

@yue

2018年學術文章

@zh

2018年學術文章

@zh-hant

name

ANXA11 mutations prevail in Chinese ALS patients with and without cognitive dementia.

@en

ANXA11 mutations prevail in Chinese ALS patients with and without cognitive dementia.

@nl

type

Item

label

ANXA11 mutations prevail in Chinese ALS patients with and without cognitive dementia.

@en

ANXA11 mutations prevail in Chinese ALS patients with and without cognitive dementia.

@nl

prefLabel

ANXA11 mutations prevail in Chinese ALS patients with and without cognitive dementia.

@en

ANXA11 mutations prevail in Chinese ALS patients with and without cognitive dementia.

@nl

P1476

ANXA11 mutations prevail in Chinese ALS patients with and without cognitive dementia.

@en

P2093

Dongchao Shen

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

Hanhui Fu

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

Hongfei Tai

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

Kang Zhang

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

Keqiang Liu

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

Liying Cui

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

Mingsheng Liu

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

Qing Liu

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

Qingyun Ding

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

Shi Shu

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

P2860

A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement

Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia

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

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

Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis

P304

e237

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

P31

scholarly article

P356

10.1212/NXG.0000000000000237

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

P433

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

P478

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

P577

2018-05-22T00:00:00Z

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

P698

29845112

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

P921

amyotrophic lateral sclerosis

P932

5963931

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