Human ABL1 deficiency syndrome (HADS) is a recognizable syndrome distinct from ABL1-related congenital heart defects and skeletal malformations syndrome
| Title: | Human ABL1 deficiency syndrome (HADS) is a recognizable syndrome distinct from ABL1-related congenital heart defects and skeletal malformations syndrome |
|---|---|
| Authors: | AlAbdi, LamaAff1; Neuhann, TeresaAff2; Prott, Eva-ChristinaAff3; Schön, UlrikeAff2; Abdulwahab, FirdousAff1; Faqeih, EissaAff4; Alkuraya, Fowzan S.Aff1, IDs0043902402677y_cor7 |
| Source: | Human Genetics. 143(6):739-745 |
| Database: | Springer Nature Journals |