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Comment
. 2014 Dec;137(Pt 12):e311.
doi: 10.1093/brain/awu265. Epub 2014 Sep 26.

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

Janel O Johnson  1 , Shannon M Glynn  1 , J Raphael Gibbs  2 , Mike A Nalls  3 , Mario Sabatelli  4 , Gabriella Restagno  5 , Vivian E Drory  6 , Adriano Chiò  7 , Ekaterina Rogaeva  8 , Bryan J Traynor  9
Affiliations
Comment

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

Janel O Johnson et al. Brain. 2014 Dec.
No abstract available

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  • Reply: Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis.
    Bannwarth S, Ait-El-Mkadem S, Chaussenot A, Genin EC, Lacas-Gervais S, Fragaki K, Berg-Alonso L, Kageyama Y, Serre V, Moore D, Verschueren A, Rouzier C, Le Ber I, Augé G, Cochaud C, Lespinasse F, N'Guyen K, de Septenville A, Brice A, Yu-Wai-Man P, Sesaki H, Pouget J, Paquis-Flucklinger V. Bannwarth S, et al. Brain. 2014 Dec;137(Pt 12):e312. doi: 10.1093/brain/awu267. Epub 2014 Sep 26. Brain. 2014. PMID: 25261971 Free PMC article. No abstract available.

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References

    1. Bannwarth S, Ait-El-Mkadem S, Chaussenot A, Genin EC, Lacas-Gervais S, Fragaki K, et al. A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement. Brain. 2014;137(Pt 8):2329–45. - PMC - PubMed
    1. Brooks BR. El Escorial World Federation of Neurology criteria for the diagnosis of amyotrophic lateral sclerosis. Subcommittee on Motor Neuron Diseases/Amyotrophic Lateral Sclerosis of the World Federation of Neurology Research Group on Neuromuscular Diseases and the El Escorial ‘Clinical limits of amyotrophic lateral sclerosis' workshop contributors. J Neurol Sci. 1994;124:96–107. - PubMed
    1. Johnson JO, Mandrioli J, Benatar M, Abramzon Y, Van Deerlin VM, Trojanowski JQ, et al. Exome sequencing reveals VCP mutations as a cause of familial ALS. Neuron. 2010;68:857–64. - PMC - PubMed
    1. Johnson JO, Pioro EP, Boehringer A, Chia R, Feit H, Renton AE, et al. Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis. Nat Neurosci. 2014;17:664–6. - PMC - PubMed
    1. Renton AE, Chiò A, Traynor BJ. State of play in amyotrophic lateral sclerosis genetics. Nat Neurosci. 2014;17:17–23. - PMC - PubMed