Cita APA

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

Citación estilo Chicago

Errasti Díaz, Suriel, Mercedes Peñalva, Lucía Recio Poveda, Susana Vilches, Juan Casado Vela, Julián Pérez Pérez, Luisa María Botella, Virginia Albiñana, y Ángel Cuesta Martínez. A Novel Splicing Mutation in the ACVRL1/ALK1 Gene As a Cause of HHT2. 2022.

Cita MLA

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