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Identification and characterization of new RNASEH1 mutations associated with PEO syndrome and multiple mitochondrial DNA deletions
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Identification and characterization of new RNASEH1 mutations associated with PEO syndrome and multiple mitochondrial DNA deletions
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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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