Published in
Elsevier, Mitochondrion, (46), p. 337-344, 2019
DOI: 10.1016/j.mito.2018.09.004
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Deep sequencing discovery of causal mtDNA mutations in a patient with unspecific neurological disease
Journal article published in 2018 by
Lucía Spangenberg,
Martín Graña 
,
Santiago Mansilla,
Jennyfer Martínez,
Alejandra Tapié,
Gonzalo Greif,
Nélida Montano,
Alicia Vaglio,
Rosario Guecaimburú,
Carlos Robello,
Laura Castro,
Celia Quijano ,
Victor Raggio,
Hugo Naya
,
Santiago Mansilla,
Jennyfer Martínez,
Alejandra Tapié,
Gonzalo Greif,
Nélida Montano,
Alicia Vaglio,
Rosario Guecaimburú,
Carlos Robello,
Laura Castro,
Celia Quijano ,
Victor Raggio,
Hugo Naya
This paper was not found in any repository, but could be made available legally by the author.
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