Barraza-Flores, P., Bukovec, K. E., Dagda, M., Conner, B. W., Oliveira-Santos, A., Grange, R. W., & Burkin, D. J. (2020). Laminin-111 protein therapy after disease onset slows muscle disease in a mouse model of laminin-α2 related congenital muscular dystrophy. Hum Mol Genet.
Citación estilo ChicagoBarraza-Flores, Pamela, Katherine E. Bukovec, Marisela Dagda, Brandon W. Conner, Ariany Oliveira-Santos, Robert W. Grange, y Dean J. Burkin. "Laminin-111 Protein Therapy After Disease Onset Slows Muscle Disease in a Mouse Model of Laminin-α2 Related Congenital Muscular Dystrophy." Hum Mol Genet 2020.
Cita MLABarraza-Flores, Pamela, et al. "Laminin-111 Protein Therapy After Disease Onset Slows Muscle Disease in a Mouse Model of Laminin-α2 Related Congenital Muscular Dystrophy." Hum Mol Genet 2020.