Gurgel-Giannetti, Juliana ;
Lynch, David S ;
Brandão de Paiva, Anderson Rodrigues...
Gurgel-Giannetti , J , Lynch , D S , Brandão de Paiva , A R , Lucato , L T , Yamamoto , G , Thomsen , C , Basu , S , Freua , F , Giannetti , A V , Ripa de Assis , B D , Ospedale Ribeiro , M D , Barcelos , I , Souza , K S , Monti , F , Melo , U S , Amorim , S , Silva , L G L , Macedo-Souza , L C I , Vianna-Morgante , A M , Hirano , M , van der Knaap , M S , Lill , R , Vainzof , M , Oldfors , A , Houlden , H & Kok , F 2018 , ' A novel complex neurological phenotype due to a homozygous mutation in FDX2 ' , Brain , vol. 141 , no. 8 , pp. 2289-2298 . https://doi.org/10.1093/brain/awy172.
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2018