Subirà, O., Català-Mora, J., Díaz-Cascajosa, J., Padrón-Pérez, N., Claveria, M. A., Coll-Alsina, N., . . . Prat, J. (2019). Retinal findings in pediatric patients with Usher syndrome Type 1 due to mutations in MYO7A gene. Eye (Lond).
Chicago Style CitationSubirà, Olaia, et al. "Retinal Findings in Pediatric Patients With Usher Syndrome Type 1 Due to Mutations in MYO7A Gene." Eye (Lond) 2019.
MLA CitationSubirà, Olaia, et al. "Retinal Findings in Pediatric Patients With Usher Syndrome Type 1 Due to Mutations in MYO7A Gene." Eye (Lond) 2019.
Warning: These citations may not always be 100% accurate.