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Identification and characterization of new RNASEH1 mutations associated with PEO syndrome and multiple mitochondrial DNA deletions - Carreño Gago, Lidia (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Blázquez-Bermejo, Cora (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Diaz-Manera, Jordi. (Institut d'Investigació Biomèdica Sant Pau) ; Cámara, Yolanda (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Gallardo, Eduard (Institut d'Investigació Biomèdica Sant Pau) ; Martí, R. (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Torres-Torronteras, J. (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Garcia-Arumi, Elena (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Universitat Autònoma de Barcelona
 
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