相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation
Delia Kurzwelly et al.
BRAIN (2015)
CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosis
Dario Ronchi et al.
BRAIN (2015)
CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients
Adriano Chio et al.
NEUROBIOLOGY OF AGING (2015)
Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease
Kathrin Mueller et al.
BRAIN (2014)
Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis
Janel O. Johnson et al.
BRAIN (2014)
A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement
Sylvie Bannwarth et al.
BRAIN (2014)
Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patients
Annabelle Chaussenot et al.
NEUROBIOLOGY OF AGING (2014)
An integrated map of genetic variation from 1,092 human genomes
David M. Altshuler et al.
NATURE (2012)
Mitochondria in Neuroplasticity and Neurological Disorders
Mark P. Mattson et al.
NEURON (2008)
分享论文
