Analysis of CHCHD2 gene in familial Parkinson's disease from Calabria-Reference-Cited by-同舟云学术

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Analysis of CHCHD2 gene in familial Parkinson's disease from Calabria

Published:2017-02 Issue: Volume:50 Page:169.e5-169.e6
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Gagliardi Monica,Iannello Grazia,Colica Carmela,Annesi Grazia,Quattrone Aldo

Publisher

Elsevier BV

Subject

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

Reference11 articles.

1. Lack of CHCHD2 mutations in Parkinson's disease in a Taiwanese population;Fan;Neurobiol. Aging,2016

2. CHCHD2 and Parkinson's disease;Foo;Lancet Neurol.,2015

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

4. CHCHD2 and Parkinson's disease;Iqbal;Lancet Neurol.,2015

5. CHCHD2 and Parkinson's disease;Jansen;Lancet Neurol.,2015

Cited by 9 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. Calabria as a Genetic Isolate: A Model for the Study of Neurodegenerative Diseases;Biomedicines;2022-09-15

2. Connecting the dots between mitochondrial dysfunction and Parkinson’s disorder: focus mitochondria-targeting therapeutic paradigm in mitigating the disease severity;Environmental Science and Pollution Research;2021-05-29

3. Mitochondrial CHCHD2: Disease-Associated Mutations, Physiological Functions, and Current Animal Models;Frontiers in Aging Neuroscience;2021-04-22

4. Mutations in CHCHD2 cause α-synuclein aggregation;Human Molecular Genetics;2019-10-10

5. Mitochondrial Dysfunction in Parkinson’s Disease—Cause or Consequence?;Biology;2019-05-11

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