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CHCHD10 mutations are not a common cause of SMN1 ‐negative type III/IV spinal motor atrophy
Author(s) -
Morel Godelieve,
Rouzier Cécile,
Chaussenot Annabelle,
AitElMkadem Samira,
Bannwarth Sylvie,
Genin Emmanuelle C.,
Augé Gaëlle,
Chabrol Brigitte,
Pouget Jean,
Soriani Marie Hélène,
Sacconi Sabrina,
PaquisFlucklinger Véronique
Publication year - 2015
Publication title -
annals of neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.764
H-Index - 296
eISSN - 1531-8249
pISSN - 0364-5134
DOI - 10.1002/ana.24464
Subject(s) - smn1 , spinal muscular atrophy , atrophy , medicine , mutation , genetics , biology , neuroscience , gene
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