Article Versions Notes

Errasti Díaz S, Peñalva M, Recio-Poveda L, Vilches S, Casado-Vela J, Pérez Pérez J, Botella LM, Albiñana V, Cuesta AM. A Novel Splicing Mutation in the ACVRL1/ALK1 Gene as a Cause of HHT2. Journal of Clinical Medicine. 2022; 11(11):3053. https://doi.org/10.3390/jcm11113053

Errasti Díaz, Suriel, Mercedes Peñalva, Lucía Recio-Poveda, Susana Vilches, Juan Casado-Vela, Julián Pérez Pérez, Luisa María Botella, Virginia Albiñana, and Angel M. Cuesta. 2022. "A Novel Splicing Mutation in the ACVRL1/ALK1 Gene as a Cause of HHT2" Journal of Clinical Medicine 11, no. 11: 3053. https://doi.org/10.3390/jcm11113053

Errasti Díaz, S., Peñalva, M., Recio-Poveda, L., Vilches, S., Casado-Vela, J., Pérez Pérez, J., Botella, L. M., Albiñana, V., & Cuesta, A. M. (2022). A Novel Splicing Mutation in the ACVRL1/ALK1 Gene as a Cause of HHT2. Journal of Clinical Medicine, 11(11), 3053. https://doi.org/10.3390/jcm11113053