C9orf72 mutation is rare in Alzheimer's disease, Parkinson's disease, and essential tremor in China-Reference-Cited by-同舟云学术

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C9orf72 mutation is rare in Alzheimer's disease, Parkinson's disease, and essential tremor in China

Published:2013 Issue: Volume:7 Page:
ISSN:1662-5102
Container-title:Frontiers in Cellular Neuroscience
language:
Short-container-title:Front. Cell. Neurosci.

Author:

Jiao Bin,Guo Ji-feng,Wang Ya-qin,Yan Xin-xiang,Zhou Lin,Liu Xiao-yan,Zhang Fu-feng,Zhou Ya-fang,Xia Kun,Tang Bei-sha,Shen Lu

Publisher

Frontiers Media SA

Subject

Cellular and Molecular Neuroscience

Cited by 33 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. Meta-analysis of the association between C9orf72 repeats and neurodegeneration diseases;Journal of Neurogenetics;2024-01-02

2. The genetic basis of multiple system atrophy;Journal of Translational Medicine;2023-02-10

3. Expanding the spectrum of C9ORF72-related neurodegenerative disorders in the Greek population;Journal of the Neurological Sciences;2022-11

4. Identification of TARDBP Gly298Ser as a founder mutation for amyotrophic lateral sclerosis in Southern China;BMC Medical Genomics;2022-08-05

5. C9orf72-G4C2 Intermediate Repeats and Parkinson’s Disease; A Data-Driven Hypothesis;Genes;2021-08-05

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