Cita APA

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

Citación estilo Chicago

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

Cita MLA

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