P453: Double heterozygous variants in ACVRL1 and GDF2 causing hereditary hemorrhagic telangiectasia and GDF2-related vascular anomaly syndrome

Autor: Girnary, Zahra, Smith, Karen, Kasthuri, Raj
Zdroj: In Genetics in Medicine Open 2024 2 Supplement 1
Databáze: ScienceDirect