Reply: Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis?
- PMID: 25348633
- PMCID: PMC4240304
- DOI: 10.1093/brain/awu300
Reply: Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis?
Comment on
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A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement.Brain. 2014 Aug;137(Pt 8):2329-45. doi: 10.1093/brain/awu138. Epub 2014 Jun 16. Brain. 2014. PMID: 24934289 Free PMC article.
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Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis?Brain. 2014 Dec;137(Pt 12):e313. doi: 10.1093/brain/awu299. Epub 2014 Oct 27. Brain. 2014. PMID: 25348631 No abstract available.
References
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- Chaussenot A, Le Ber I, Ait-El-Mkadem S, Camuzat A, de Septenville A, Bannwarth S, et al. Screening of CHCHD10 in a French cohort confirms the involvement of this gene in FTD-ALS. Neurobiol Aging. 2014 S0197-4580(14)00491-6. - PubMed
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- Leblond CS, Kaneb HM, Dion PA, Rouleau GA. Dissection of genetic factors associated with amyotrophic lateral sclerosis. Exp Neurol. 2014 S0014-4886(14)00115-0. - PubMed
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- Mueller K, Andersen P, Hübers A, Marroquin N, Volk A, Danzer K, et al. Two novel mutations in conserved codons indicate that CHCHD10 is a motor neuron disease gene. Brain. 2014 doi: 10.1093/brain/awu227. - PubMed
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