Mutation screening in Chinese patients with familial Alzheimer's disease by whole-exome sequencing-Reference-Cited by-同舟云学术

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Mutation screening in Chinese patients with familial Alzheimer's disease by whole-exome sequencing

Published:2019-04 Issue: Volume:76 Page:215.e15-215.e21
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Jiang Bin,Zhou Jiong,Li Hong-Lei,Chen Yan-Gui,Cheng Hong-Rong,Ye Ling-Qi^ORCID,Liu De-Shan,Chen Dian-Fu,Tao Qing-Qing,Wu Zhi-Ying

Funder

Key Research and Development project of Zhejiang Province

Zhejiang University

National Natural Science Foundation of China

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Neurology (clinical),Aging,General Neuroscience

Reference47 articles.

1. Diagnostic and statistical manual of mental disorders;American Psychiatric Association,2000

2. Genetics of Alzheimer disease;Bekris;J. Geriatr. Psychiatry Neurol.,2010

3. Late onset familial Alzheimer's disease: novel presenilin 2 mutation and PS1 E318G polymorphism;Bernardi;J. Neurol.,2008

4. Molecular genetics of early-onset Alzheimer's disease revisited;Cacace;Alzheimers Dement.,2016

5. Mutations in presenilin 2 and its implications in Alzheimer's disease and other dementia-associated disorders;Cai;Clin. Interv. Aging,2015

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