Mutational analysis of CHCHD2 in Chinese patients with multiple system atrophy and amyotrophic lateral sclerosis-Reference-Cited by-同舟云学术

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Mutational analysis of CHCHD2 in Chinese patients with multiple system atrophy and amyotrophic lateral sclerosis

Published:2016-09 Issue: Volume:368 Page:389-391
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Yang Xinglong,An Ran,Zhao Quanzhen,Zheng Jinhua,Tian Sijia,Chen Yalan,Xu Yanming

Funder

Sichuan Key Project of Science and Technology

Sichuan Province Applied Basic Research Program

National Natural Science Foundation of China

China Scholarship Council

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

Reference25 articles.

1. Mitochondrial dysfunction in Parkinson's disease;Moon;Exp. Neurobiol.,2015

2. Mitochondrial dynamism and the pathogenesis of Amyotrophic Lateral Sclerosis;Cozzolino;Front. Cell. Neurosci.,2015

3. Mitochondrial respiratory chain function in multiple system atrophy;Gu;Mov. Disord.,1997

4. Grossman LI.MNRR1 (formerly CHCHD2) is bio-organellar regulator of mitochondrial metabolism;Aras;Mitochondrion,2015

5. CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study;Funayama;Lancet Neurol.,2015

Cited by 8 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. The genetic basis of multiple system atrophy;Journal of Translational Medicine;2023-02-10

2. Cross-examining candidate genes implicated in multiple system atrophy;Acta Neuropathologica Communications;2019-07-24

3. Limb girdle muscular dystrophy D3 HNRNPDL related in a Chinese family with distal muscle weakness caused by a mutation in the prion-like domain;Journal of Neurology;2019-01-02

4. CHCHD2 promotes hepatocellular carcinoma and indicates poor prognosis of hepatocellular carcinoma patients;Journal of Cancer;2019

5. A new CHCHD2 mutation identified in a southern italy patient with multiple system atrophy;Parkinsonism & Related Disorders;2018-02

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