Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation

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/awv015

Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation

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

3 Scopus citations

Original language	English (US)
Pages (from-to)	e377
Journal	Brain
Volume	138
Issue number	9
DOIs	https://doi.org/10.1093/brain/awv015
State	Published - Sep 1 2015

ASJC Scopus subject areas

Medicine(all)

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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. (2015). Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation. Brain, 138(9), e377. https://doi.org/10.1093/brain/awv015

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 2015, 'Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation', Brain, vol. 138, no. 9, pp. e377. https://doi.org/10.1093/brain/awv015

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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",

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AU - Lacas-Gervais, Sandra

AU - Fragaki, Konstantina

AU - Berg-Alonso, Laetitia

AU - Kageyama, Yusuke

AU - Serre, Valérie

AU - Moore, David

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AU - Rouzier, Cécile

AU - Le Ber, Isabelle

AU - Augé, Gaëlle

AU - Cochaud, Charlotte

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AU - N'Guyen, Karine

AU - De Septenville, Anne

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Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation

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