Reduced penetrance of the PSEN1 H163Y autosomal dominant Alzheimer mutation: a 22-year follow-up study.

about

Reduced penetrance of the PSEN1 H163Y autosomal dominant Alzheimer mutation: a 22-year follow-up study.

Item

http://www.wikidata.org/entity/Q55178076

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

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-hant

name

Reduced penetrance of the PSEN ...... on: a 22-year follow-up study.

@en

Reduced penetrance of the PSEN ...... on: a 22-year follow-up study.

@nl

type

Item

label

Reduced penetrance of the PSEN ...... on: a 22-year follow-up study.

@en

Reduced penetrance of the PSEN ...... on: a 22-year follow-up study.

@nl

prefLabel

Reduced penetrance of the PSEN ...... on: a 22-year follow-up study.

@en

Reduced penetrance of the PSEN ...... on: a 22-year follow-up study.

@nl

P1476

Reduced penetrance of the PSEN ...... on: a 22-year follow-up study.

@en

P2093

Anders Wall

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

Anne Kinhult-Ståhlbom

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

Daniel Ferreira

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

Elena Rodriguez-Vieitez

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

Håkan Thonberg

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

Laure Saint-Aubert

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

Michael Schöll

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

Steinunn Thordardottir

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

P2860

The genetic epidemiology of neurodegenerative disease.

Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

Toward defining the preclinical stages of Alzheimer's disease: recommendations from the National Institute on Aging-Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease

The amyloid hypothesis of Alzheimer's disease at 25 years

Genetic heterogeneity in Alzheimer disease and implications for treatment strategies

Neuropathological stageing of Alzheimer-related changes

Cortical Surface-Based Analysis

Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease

Early-onset Alzheimer's disease caused by mutations at codon 717 of the beta-amyloid precursor protein gene

Clinical phenotypic heterogeneity of Alzheimer's disease associated with mutations of the presenilin-1 gene

P2888

s13195-018-0374-y

P304

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

P31

scholarly article

P356

10.1186/S13195-018-0374-Y

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

P407

English

P433

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

P478

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

P50

P577

2018-05-10T00:00:00Z

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

P6179

1103934862

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

P698

29747683

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

P932

5944151

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