APA
Castro-Gago M., Dacruz-Alvarez D., Pintos-Martínez E., Beiras-Iglesias A., Delmiro A., Arenas J., Martín M. Á. & Martínez-Azorín F. (20150710). Exome sequencing identifies a CHKB mutation in Spanish patient with megaconial congenital muscular dystrophy and mtDNA depletion. : European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
Chicago
Castro-Gago Manuel, Dacruz-Alvarez David, Pintos-Martínez Elena, Beiras-Iglesias Andrés, Delmiro Aitor, Arenas Joaquín, Martín Miguel Ángel and Martínez-Azorín Francisco. 20150710. Exome sequencing identifies a CHKB mutation in Spanish patient with megaconial congenital muscular dystrophy and mtDNA depletion. : European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
Harvard
Castro-Gago M., Dacruz-Alvarez D., Pintos-Martínez E., Beiras-Iglesias A., Delmiro A., Arenas J., Martín M. Á. and Martínez-Azorín F. (20150710). Exome sequencing identifies a CHKB mutation in Spanish patient with megaconial congenital muscular dystrophy and mtDNA depletion. : European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
MLA
Castro-Gago Manuel, Dacruz-Alvarez David, Pintos-Martínez Elena, Beiras-Iglesias Andrés, Delmiro Aitor, Arenas Joaquín, Martín Miguel Ángel and Martínez-Azorín Francisco. Exome sequencing identifies a CHKB mutation in Spanish patient with megaconial congenital muscular dystrophy and mtDNA depletion. : European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society. 20150710.