Mutation analysis ofCHCHD10in different neurodegenerative diseases-Reference-Cited by-同舟云学术

Mutation analysis ofCHCHD10in different neurodegenerative diseases

Published:2015-03-31 Issue:9 Volume:138 Page:e380-e380
ISSN:0006-8950
Container-title:Brain
language:en
Short-container-title:Brain

Author:

Zhang Ming,Xi Zhengrui,Zinman Lorne,Bruni Amalia C.,Maletta Raffaele G.,Curcio Sabrina A. M.,Rainero Innocenzo,Rubino Elisa,Pinessi Lorenzo,Nacmias Benedetta,Sorbi Sandro,Galimberti Daniela,Lang Anthony E.,Fox Susan,Surace Ezequiel I.,Ghani Mahdi,Guo Jing,Sato Christine,Moreno Danielle,Liang Yan,Keith Julia,Traynor Bryan J.,St George-Hyslop Peter,Rogaeva Ekaterina

Publisher

Oxford University Press (OUP)

Subject

Clinical Neurology

Link

http://academic.oup.com/brain/article-pdf/138/9/e380/11141559/awv082.pdf

Reference10 articles.

1. Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathy

2. A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement

3. Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patients

4. Mitochondria and ALS: Implications from novel genes and pathways

5. CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study

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