Open AccessReply: Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis
Author(s) -
Sylvie Bannwarth,
Samira Ait-El-Mkadem,
Annabelle Chaussenot,
Emmanuelle C. Genin,
Sandra LacasGervais,
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 Nguyen,
Anne de Septenville,
Alexis Brice,
Patrick YuWaiMan,
Hiromi Sesaki,
Jean Pouget,
Véronique PaquisFlucklinger
Publication year - 2014
Publication title -
brain
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.142
H-Index - 336
eISSN - 1460-2156
pISSN - 0006-8950
DOI - 10.1093/brain/awu267
Subject(s) - amyotrophic lateral sclerosis , genetics , gene , mutation , medicine , biology , disease , pathology
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom