CHCHD10 is not a frequent causative gene in Chinese ALS patients

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The cellular stress proteins CHCHD10 and MNRR1 (CHCHD2): Partners in mitochondrial and nuclear function and dysfunction.

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CHCHD10 is not a frequent causative gene in Chinese ALS patients

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wetenschappelijk artikel

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наукова стаття, опублікована у квітні 2016

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CHCHD10 is not a frequent causative gene in Chinese ALS patients

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CHCHD10 is not a frequent causative gene in Chinese ALS patients

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CHCHD10 is not a frequent causative gene in Chinese ALS patients

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CHCHD10 is not a frequent causative gene in Chinese ALS patients

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CHCHD10 is not a frequent causative gene in Chinese ALS patients

@en

CHCHD10 is not a frequent causative gene in Chinese ALS patients

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CHCHD10 is not a frequent causative gene in Chinese ALS patients

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Bin Peng

http://www.w3.org/2001/XMLSchema#string

Bo Cui

http://www.w3.org/2001/XMLSchema#string

Fang Liu

http://www.w3.org/2001/XMLSchema#string

Li Ying Cui

http://www.w3.org/2001/XMLSchema#string

Ming Sheng Liu

http://www.w3.org/2001/XMLSchema#string

Qing Liu

http://www.w3.org/2001/XMLSchema#string

Shi Shu

http://www.w3.org/2001/XMLSchema#string

Xiao Guang Li

http://www.w3.org/2001/XMLSchema#string

Xiao Ling Li

http://www.w3.org/2001/XMLSchema#string

Xue Zhang

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

El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis

Genetic epidemiology of amyotrophic lateral sclerosis.

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

Mitochondrial dysfunction is a converging point of multiple pathological pathways in amyotrophic lateral sclerosis.

Clinical genetics of amyotrophic lateral sclerosis: what do we really know?

Mitochondria and ALS: implications from novel genes and pathways.

Intrafamilial clinical variability in individuals carrying the CHCHD10 mutation Gly66Val.

Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis.

Analysis of the CHCHD10 gene in patients with frontotemporal dementia and amyotrophic lateral sclerosis from Spain.

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458-460

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scholarly article

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10.3109/21678421.2016.1170151

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5-6

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2016-04-14T00:00:00Z

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27077676

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amyotrophic lateral sclerosis

CHCHD10 is not a frequent causative gene in Chinese ALS patients

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CHCHD10 is not a frequent causative gene in Chinese ALS patients

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P1476

P2093

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P304

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P356

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