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Comment
. 2014 Dec;137(Pt 12):e312.
doi: 10.1093/brain/awu267. Epub 2014 Sep 26.

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

Sylvie Bannwarth  1 , Samira Ait-El-Mkadem  1 , Annabelle Chaussenot  1 , Emmanuelle C Genin  2 , Sandra Lacas-Gervais  3 , Konstantina Fragaki  1 , Laetitia Berg-Alonso  2 , Yusuke Kageyama  4 , Valérie Serre  5 , David Moore  6 , Annie Verschueren  7 , Cécile Rouzier  1 , Isabelle Le Ber  8 , Gaëlle Augé  1 , Charlotte Cochaud  9 , Françoise Lespinasse  2 , Karine N'Guyen  10 , Anne de Septenville  11 , Alexis Brice  11 , Patrick Yu-Wai-Man  12 , Hiromi Sesaki  4 , Jean Pouget  7 , Véronique Paquis-Flucklinger  13
Affiliations
Comment

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

Sylvie Bannwarth et al. Brain. 2014 Dec.
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;137:2329–45. - PMC - PubMed
    1. 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 http://dx.doi.org/10.1016/j.neurobiolaging.2014.07.022. - DOI - PubMed
    1. Johnson J, Glynn S, Gibbs J, Nalls M, Sabatelli M, Restagno G, et al. Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis. Brain. 2014;137:e311. - PMC - PubMed
    1. Müeller 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;137:e309. - PubMed