Functional and splicing defect analysis of 23 ACVRL1 mutations in a cohort of patients affected by Hereditary Hemorrhagic Telangiectasia.
PloS one | 2015-01-01 | PMID 26176610
Alaa El Din Ferdos, Patri Sylvie, Thoreau Vincent and 6 more
Genes: ACVRL1, ENG
