Published in
Oxford University Press, Brain, 8(141), p. 2289-2298, 2018
DOI: 10.1093/brain/awy172
Links
Tools
A novel complex neurological phenotype due to a homozygous mutation in FDX2
Journal article published in 2018 by
Juliana Gurgel-Giannetti,
David S. Lynch,
Anderson Rodrigues Brandão de Paiva,
Leandro Tavares Lucato,
Guilherme Yamamoto,
Christer Thomsen,
Somsuvro Basu,
Fernando Freua,
Alexandre Varella Giannetti,
Bruno Della Ripa de Assis,
Mara Dell Ospedale Ribeiro,
Isabella Barcelos,
Katiane Sayão Souza,
Fernanda Monti,
Uirá Souto Melo 
and other authors.
and other authors.
This paper was not found in any repository, but could be made available legally by the author.
Full text: Unavailable
Published version:
archiving forbidden
Data provided by 