Related references
Note: Only part of the references are listed.Is CHCHD10 Pro34Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis?
Carol Dobson-Stone et al.
BRAIN (2015)
Reply: Is CHCHD10 Pro34Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis?
Sylvie Bannwarth et al.
BRAIN (2015)
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)
Mutation analysis of CHCHD10 in different neurodegenerative diseases
Ming Zhang 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)
Late Onset Spinal Motor Neuronopathy Is Caused by Mutation in CHCHD10
Sini Penttila et al.
ANNALS OF NEUROLOGY (2015)
Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathy
Senda Ajroud-Driss et al.
NEUROGENETICS (2015)
CHCHD10 variant p.(Gly66Val) causes axonal Charcot-Marie-Tooth disease
Mari Auranen et al.
NEUROLOGY-GENETICS (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)
Targeted next-generation sequencing reveals further genetic heterogeneity in axonal Charcot-Marie-Tooth neuropathy and a mutation in HSPB1
Emil Ylikallio et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (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)
Mitofusin 2 mutations affect mitochondrial function by mitochondrial DNA depletion
Stefan Vielhaber et al.
ACTA NEUROPATHOLOGICA (2013)
The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype
Cecile Rouzier et al.
BRAIN (2012)
Autosomal dominant late-onset spinal motor neuronopathy is linked to a new locus on chromosome 22q11.2-q13.2
Sini Penttila et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2012)
Mitofusin 2 is necessary for striatal axonal projections of midbrain dopamine neurons
Seungmin Lee et al.
HUMAN MOLECULAR GENETICS (2012)
Late-onset lower motor neuronopathy A new autosomal dominant disorder
M. Jokela et al.
NEUROLOGY (2011)
Early onset severe and late-onset mild Charcot-Marie-Tooth disease with mitofusin 2 (MFN2) mutations
K. W. Chung et al.
BRAIN (2006)
Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2
S Züchner et al.
ANNALS OF NEUROLOGY (2006)
Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A
S Züchner et al.
NATURE GENETICS (2004)
Share Paper
