Reply

Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis?

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, Cochaud Charlotte, Françoise Lespinasse, Karine N'Guyen, Anne De Septenville, Alexis Brice, Patrick Yu-Wai-Man & 3 others Hiromi Sesaki, Jean Pouget, Véronique Paquis-Flucklinger

Research output: Contribution to journal › Article

Original languageEnglish (US)
Pages (from-to)e314
JournalBrain
Volume137
Issue number12
DOIs
StatePublished - Dec 1 2014

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Mutation
Amyotrophic Lateral Sclerosis
Familial
Frontotemporal Dementia
Mitochondria
Mitochondrial DNA

ASJC Scopus subject areas

  • Clinical Neurology
  • Arts and Humanities (miscellaneous)
  • Medicine(all)

Cite this

Bannwarth, S., Ait-El-Mkadem, S., Chaussenot, A., Genin, E. C., Lacas-Gervais, S., Fragaki, K., ... Paquis-Flucklinger, V. (2014). Reply: Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis? Brain, 137(12), e314. https://doi.org/10.1093/brain/awu300

Reply : Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis? / 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; Charlotte, Cochaud; 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. e314.

Research output: Contribution to journal › Article

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, Charlotte, C, Lespinasse, F, N'Guyen, K, De Septenville, A, Brice, A, Yu-Wai-Man, P, Sesaki, H, Pouget, J & Paquis-Flucklinger, V 2014, 'Reply: Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis?', Brain, vol. 137, no. 12, pp. e314. https://doi.org/10.1093/brain/awu300
Bannwarth S, Ait-El-Mkadem S, Chaussenot A, Genin EC, Lacas-Gervais S, Fragaki K et al. Reply: Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis? Brain. 2014 Dec 1;137(12):e314. https://doi.org/10.1093/brain/awu300
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 ; Charlotte, Cochaud ; Lespinasse, Françoise ; N'Guyen, Karine ; De Septenville, Anne ; Brice, Alexis ; Yu-Wai-Man, Patrick ; Sesaki, Hiromi ; Pouget, Jean ; Paquis-Flucklinger, Véronique. / Reply : Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis?. In: Brain. 2014 ; Vol. 137, No. 12. pp. e314.
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