Original language | English (US) |
---|---|
Pages (from-to) | e314 |
Journal | Brain |
Volume | 137 |
Issue number | 12 |
DOIs | |
State | Published - Dec 1 2014 |
ASJC Scopus subject areas
- Clinical Neurology
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In: Brain, Vol. 137, No. 12, 01.12.2014, p. e314.
Research output: Contribution to journal › Letter › peer-review
}
TY - JOUR
T1 - Reply
T2 - Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis?
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 - Charlotte, Cochaud
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).
PY - 2014/12/1
Y1 - 2014/12/1
UR - http://www.scopus.com/inward/record.url?scp=84922368579&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84922368579&partnerID=8YFLogxK
U2 - 10.1093/brain/awu300
DO - 10.1093/brain/awu300
M3 - Letter
C2 - 25348633
AN - SCOPUS:84922368579
SN - 0006-8950
VL - 137
SP - e314
JO - Brain
JF - Brain
IS - 12
ER -