Publikationen in Zusammenarbeit mit Forschern von Hospital Universitario Central de Asturias (2)

2017

  1. Myopathic mtDNA depletion syndrome due to mutation in TK2 Gene

    Pediatric and Developmental Pathology, Vol. 20, Núm. 5, pp. 416-420

2011

  1. Biochemical parameters to assess choroid plexus dysfunction in Kearns-Sayre syndrome patients

    Mitochondrion, Vol. 11, Núm. 6, pp. 867-870