Cita APA

Aguilera, C., Esteve Garcia, A., Casasnovas, C., Vélez Santamaría, V., Rausell, L., Gargallo, P., . . . Padró Miquel, A. (2023). Novel intragenic deletion within the FXN gene in a patient with typical phenotype of Friedreich ataxia: May be more prevalent than we think?

Citación estilo Chicago

Aguilera, Cinthia, et al. Novel Intragenic Deletion Within the FXN Gene in a Patient With Typical Phenotype of Friedreich Ataxia: May Be More Prevalent Than We Think? 2023.

Cita MLA

Aguilera, Cinthia, et al. Novel Intragenic Deletion Within the FXN Gene in a Patient With Typical Phenotype of Friedreich Ataxia: May Be More Prevalent Than We Think? 2023.