Reply: Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease

Sylvie Bannwarth; Samira Ait-El-Mkadem; Annabelle Chaussenot; Emmanuelle C. Genin; Sandra Lacas-Gervais; Konstantina Fragaki; Laetitia Berg-Alonso; Yusuke Kageyama; Valérie Serre; David Moore; Annie Verschueren; Cécile Rouzier; Isabelle Le Ber; Gaëlle Augé; Charlotte Cochaud; Françoise Lespinasse; Karine N'Guyen; Anne De Septenville; Alexis Brice; Patrick Yu-Wai-Man; Hiromi Sesaki; Jean Pouget; Véronique Paquis-Flucklinger

doi:10.1093/brain/awu228

Reply: Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease

Sylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, Emmanuelle C. Genin, Sandra Lacas-Gervais, Konstantina Fragaki, Laetitia Berg-Alonso, Yusuke Kageyama, Valérie Serre, David Moore, Annie Verschueren, Cécile Rouzier, Isabelle Le Ber, Gaëlle Augé, Charlotte Cochaud, Françoise Lespinasse, Karine N'Guyen, Anne De Septenville, Alexis Brice, Patrick Yu-Wai-ManHiromi Sesaki, Jean Pouget, Véronique Paquis-Flucklinger

School of Medicine

Research output: Contribution to journal › Letter › peer-review

Original language	English (US)
Pages (from-to)	e310
Journal	Brain
Volume	137
Issue number	12
DOIs	https://doi.org/10.1093/brain/awu228
State	Published - Dec 1 2014

ASJC Scopus subject areas

Clinical Neurology

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10.1093/brain/awu228

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Bannwarth, S., Ait-El-Mkadem, S., Chaussenot, A., Genin, E. C., 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., ... Paquis-Flucklinger, V. (2014). Reply: Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease. Brain, 137(12), e310. https://doi.org/10.1093/brain/awu228

Reply : Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease. / Bannwarth, Sylvie; Ait-El-Mkadem, Samira; Chaussenot, Annabelle; Genin, Emmanuelle C.; Lacas-Gervais, Sandra; Fragaki, Konstantina; Berg-Alonso, Laetitia; Kageyama, Yusuke; Serre, Valérie; Moore, David; Verschueren, Annie; Rouzier, Cécile; Le Ber, Isabelle; Augé, Gaëlle; Cochaud, Charlotte; Lespinasse, Françoise; N'Guyen, Karine; De Septenville, Anne; Brice, Alexis; Yu-Wai-Man, Patrick; Sesaki, Hiromi; Pouget, Jean; Paquis-Flucklinger, Véronique.

In: Brain, Vol. 137, No. 12, 01.12.2014, p. e310.

Research output: Contribution to journal › Letter › peer-review

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 2014, 'Reply: Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease', Brain, vol. 137, no. 12, pp. e310. https://doi.org/10.1093/brain/awu228

Bannwarth, Sylvie ; Ait-El-Mkadem, Samira ; Chaussenot, Annabelle ; Genin, Emmanuelle C. ; Lacas-Gervais, Sandra ; Fragaki, Konstantina ; Berg-Alonso, Laetitia ; Kageyama, Yusuke ; Serre, Valérie ; Moore, David ; Verschueren, Annie ; Rouzier, Cécile ; Le Ber, Isabelle ; Augé, Gaëlle ; Cochaud, Charlotte ; Lespinasse, Françoise ; N'Guyen, Karine ; De Septenville, Anne ; Brice, Alexis ; Yu-Wai-Man, Patrick ; Sesaki, Hiromi ; Pouget, Jean ; Paquis-Flucklinger, Véronique. / Reply : Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease. In: Brain. 2014 ; Vol. 137, No. 12. pp. e310.

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title = "Reply: Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease",

author = "Sylvie Bannwarth and Samira Ait-El-Mkadem and Annabelle Chaussenot and Genin, {Emmanuelle C.} and Sandra Lacas-Gervais and Konstantina Fragaki and Laetitia Berg-Alonso and Yusuke Kageyama and Val{\'e}rie Serre and David Moore and Annie Verschueren and C{\'e}cile Rouzier and {Le Ber}, Isabelle and Ga{\"e}lle Aug{\'e} and Charlotte Cochaud and Fran{\c c}oise Lespinasse and Karine N'Guyen and {De Septenville}, Anne and Alexis Brice and Patrick Yu-Wai-Man and Hiromi Sesaki and Jean Pouget and V{\'e}ronique Paquis-Flucklinger",

note = "Funding Information: This work was made possible by grants to V.P-F from the Association Franc¸aise contre les Myopathies (AFM) and the Fondation pour la Recherche M{\'e}dicale (FRM), to H.S from National Institutes of Health (GM089853) and to A.B. by the program “Investissements d{\textquoteright}avenir” ANR-10-IAIHU-06, {\textquoteleft}The Programme Hospitalier de Recherche Clinique{\textquoteright} (to I.L.B.) and the 7th framework program of the European Union (FP7, E12009DD, Neuromics). P.Y.W.M. is supported by a Clinician Scientist Fellowship Award (G1002570) from the Medical Research Council (UK).",

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AU - Bannwarth, Sylvie

AU - Ait-El-Mkadem, Samira

AU - Chaussenot, Annabelle

AU - Genin, Emmanuelle C.

AU - Lacas-Gervais, Sandra

AU - Fragaki, Konstantina

AU - Berg-Alonso, Laetitia

AU - Kageyama, Yusuke

AU - Serre, Valérie

AU - Moore, David

AU - Verschueren, Annie

AU - Rouzier, Cécile

AU - Le Ber, Isabelle

AU - Augé, Gaëlle

AU - Cochaud, Charlotte

AU - Lespinasse, Françoise

AU - N'Guyen, Karine

AU - De Septenville, Anne

AU - Brice, Alexis

AU - Yu-Wai-Man, Patrick

AU - Sesaki, Hiromi

AU - Pouget, Jean

AU - Paquis-Flucklinger, Véronique

N1 - Funding Information: This work was made possible by grants to V.P-F from the Association Franc¸aise contre les Myopathies (AFM) and the Fondation pour la Recherche Médicale (FRM), to H.S from National Institutes of Health (GM089853) and to A.B. by the program “Investissements d’avenir” ANR-10-IAIHU-06, ‘The Programme Hospitalier de Recherche Clinique’ (to I.L.B.) and the 7th framework program of the European Union (FP7, E12009DD, Neuromics). P.Y.W.M. is supported by a Clinician Scientist Fellowship Award (G1002570) from the Medical Research Council (UK).

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JO - Brain

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Reply: Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease

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