Cita APA (7a ed.)

Estañ, M. C., Fernández-Núñez, E., Zaki, M. S., Esteban, M. I., Donkervoort, S., Hawkins, C., . . . Ruiz-Perez, V. L. (2019). Recessive mutations in muscle-specific isoforms of FXR1 cause congenital multi-minicore myopathy. Nature Portfolio.

Cita Chicago Style (17a ed.)

Estañ, María Cristina, et al. Recessive Mutations in Muscle-specific Isoforms of FXR1 Cause Congenital Multi-minicore Myopathy. Nature Portfolio, 2019.

Cita MLA (8a ed.)

Estañ, María Cristina, et al. Recessive Mutations in Muscle-specific Isoforms of FXR1 Cause Congenital Multi-minicore Myopathy. Nature Portfolio, 2019.