Deep sequencing discovery of causal mtDNA mutations in a patient with unspecific neurological disease.
Spangenberg L, Graña M, Mansilla S, Martínez J, Tapié A, Greif G, Montano N, Vaglio A, Gueçaimburú R, Robello C, Castro L, Quijano C, Raggio V, Naya H.
Spangenberg L, et al. Among authors: naya h.
Mitochondrion. 2019 May;46:337-344. doi: 10.1016/j.mito.2018.09.004. Epub 2018 Sep 15.
Mitochondrion. 2019.
PMID: 30227252