APA
Martín-Hernández E., García-Silva M. T., Quijada-Fraile P., Rodríguez-García M. E., Rivera H., Hernández-Laín A., Coca-Robinot D., Fernández-Toral J., Arenas J., Martín M. A. & Martínez-Azorín F. (20190521). Myopathic mtDNA Depletion Syndrome Due to Mutation in TK2 Gene. : Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.
Chicago
Martín-Hernández Elena, García-Silva María Teresa, Quijada-Fraile Pilar, Rodríguez-García María Elena, Rivera Henry, Hernández-Laín Aurelio, Coca-Robinot David, Fernández-Toral Joaquín, Arenas Joaquín, Martín Miguel A and Martínez-Azorín Francisco. 20190521. Myopathic mtDNA Depletion Syndrome Due to Mutation in TK2 Gene. : Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.
Harvard
Martín-Hernández E., García-Silva M. T., Quijada-Fraile P., Rodríguez-García M. E., Rivera H., Hernández-Laín A., Coca-Robinot D., Fernández-Toral J., Arenas J., Martín M. A. and Martínez-Azorín F. (20190521). Myopathic mtDNA Depletion Syndrome Due to Mutation in TK2 Gene. : Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.
MLA
Martín-Hernández Elena, García-Silva María Teresa, Quijada-Fraile Pilar, Rodríguez-García María Elena, Rivera Henry, Hernández-Laín Aurelio, Coca-Robinot David, Fernández-Toral Joaquín, Arenas Joaquín, Martín Miguel A and Martínez-Azorín Francisco. Myopathic mtDNA Depletion Syndrome Due to Mutation in TK2 Gene. : Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society. 20190521.