8q21.11 microdeletion syndrome: Delineation of HEY1 as a candidate gene in neurodevelopmental and cardiac defects
CONCLUSION: HEY1 is a candidate gene for both neurological and cardiac features of the 8q21.11 microdeletion syndrome and might, therefore, explain specific components of its pathophysiology.PMID:34549899 | DOI:10.1002/mgg3.1811
Source: Molecular Medicine - Category: Molecular Biology Authors: Ikhlas Ben Ayed Amal Bouzid Fatma Kammoun Amal Souissi Olfa Jallouli Salma Mallouli Souhir Guidara Salma Loukil Hajer Aloulou Fida Jbeli Sahar Aouichaoui Dorra Abid Fatma Abdelhedi Chahnez Triki Hassen Kamoun Saber Masmoudi Source Type: research
More News: Atrial Septal Defect | Brain | Cardiology | Disability | Genetics | Heart | Hole in the Heart | Microdeletion Syndromes | Molecular Biology | Neurology | Perinatology & Neonatology | Stem Cell Therapy | Stem Cells | Study | Translocation