Cita APA

Errasti-Díaz, S., Peñalva, M., Recio-Poveda, L., Vilches, S., Casado-Vela, J., Pérez Pérez, J., . . . Cuesta, A. (2022). A Novel Splicing Mutation in the ACVRL1/ALK1 Gene as a Cause of HHT2.

Citación estilo Chicago

Errasti-Díaz, S., M. Peñalva, L. Recio-Poveda, S. Vilches, J. Casado-Vela, J. Pérez Pérez, LM Botella, V. Albiñana, y AM Cuesta. A Novel Splicing Mutation in the ACVRL1/ALK1 Gene As a Cause of HHT2. 2022.

Cita MLA

Errasti-Díaz, S., et al. A Novel Splicing Mutation in the ACVRL1/ALK1 Gene As a Cause of HHT2. 2022.