Identification of a Novel Hemizygous SQSTM1 Nonsense Mutation in Atypical Behavioral Variant Frontotemporal Dementia-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Identification of a Novel Hemizygous SQSTM1 Nonsense Mutation in Atypical Behavioral Variant Frontotemporal Dementia

Published:2018-02-06 Issue: Volume:10 Page:
ISSN:1663-4365
Container-title:Frontiers in Aging Neuroscience
language:
Short-container-title:Front. Aging Neurosci.

Author:

Sun Lin,Rong Zhouyi,Li Wei,Zheng Honghua,Xiao Shifu,Li Xia

Funder

National Natural Science Foundation of China

Natural Science Foundation of Guangdong Province

Department of Education, Fujian Province

Publisher

Frontiers Media SA

Subject

Cognitive Neuroscience,Aging

Reference21 articles.

1. A phenotype of atypical apraxia of speech in a family carrying SQSTM1 mutation;Boutoleau-Bretonnière;J. Alzheimers. Dis.,2015

2. Paget's disease of bone in the French population: novel SQSTM1 mutations, functional analysis, and genotype-phenotype correlations;Collet;J. Bone Miner. Res.,2007

3. SQSTM1 mutations in familial and sporadic amyotrophic lateral sclerosis;Fecto;Arch. Neurol.,2011

4. Apolipoprotein-E genotyping in Alzheimer's disease and frontotemporal dementia;Gustafson;Dement. Geriatr. Cogn. Disord.,1997

5. Absence of the autophagy adaptor SQSTM1/p62 causes childhood-onset neurodegeneration with ataxia, dystonia, and gaze palsy;Haack;Am. J. Hum. Genet.,2016

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Frameshift mutation in SQSTM1 causes proximal myopathy with rimmed vacuoles: A case report;Frontiers in Neurology;2023-03-14

2. Mapping the genetic landscape of early-onset Alzheimer’s disease in a cohort of 36 families;Alzheimer's Research & Therapy;2022-06-01

3. Modelling amyotrophic lateral sclerosis in rodents;Nature Reviews Neuroscience;2022-03-08

4. Analysis of Genotype-Phenotype Correlations in Patients With Degenerative Dementia Through the Whole Exome Sequencing;Frontiers in Aging Neuroscience;2021-10-14

5. Detection of the SQSTM1 Mutation in a Patient with Early-Onset Hippocampal Amnestic Syndrome;Journal of Alzheimer's Disease;2021-01-19

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3