A Novel Splicing Mutation in the ACVRL1/ALK1 Gene as a Cause of HHT2.
Errasti Díaz S, Peñalva M, Recio-Poveda L, Vilches S, Casado-Vela J, Pérez Pérez J, Botella LM, Albiñana V, Cuesta AM.
Errasti Díaz S, et al. Among authors: cuesta am.
J Clin Med. 2022 May 28;11(11):3053. doi: 10.3390/jcm11113053.
J Clin Med. 2022.
PMID: 35683441
Free PMC article.