Open AccessReply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying aCHCHD10mutation: Table 1
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 - 2015
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/awv015
Subject(s) - amyotrophic lateral sclerosis , frontotemporal dementia , genetics , german , mutation , dementia , tardbp , disease , gene , biology , medicine , pathology , history , archaeology
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