Cita APA

Medina Carbonero, M., Sanz Alcázar, A., Britti, E., Delaspre, F., Cabiscol Català, E., Ros Salvador, J., & Tamarit Sumalla, J. (2022). Mice harboring the FXN I151F pathological point mutation present decreased frataxin levels, a Friedreich ataxia-like phenotype, and mitochondrial alterations.

Citación estilo Chicago

Medina Carbonero, Marta, Arabela Sanz Alcázar, Elena Britti, Fabien Delaspre, Elisa Cabiscol Català, Joaquim Ros Salvador, y Jordi Tamarit Sumalla. Mice Harboring the FXN I151F Pathological Point Mutation Present Decreased Frataxin Levels, a Friedreich Ataxia-like Phenotype, and Mitochondrial Alterations. 2022.

Cita MLA

Medina Carbonero, Marta, et al. Mice Harboring the FXN I151F Pathological Point Mutation Present Decreased Frataxin Levels, a Friedreich Ataxia-like Phenotype, and Mitochondrial Alterations. 2022.