Cita APA

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

Citación estilo Chicago

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

Cita MLA

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