Haploinsufficient variants in SMAD5 are associated with isolated congenital heart disease
SMAD5基因的单倍体不足变异与孤立性先天性心脏病相关
期刊:HGG Advances
影响因子:
doi:10.1016/j.xhgg.2025.100478
Alankarage, Dimuthu; Leshchynska, Iryna; Portelli, Stephanie; Sipka, Alena; Blue, Gillian M; O'Reilly, Victoria; Das, Debjani; Rath, Emma M; Enriquez, Annabelle; Troup, Michael; Fine, Miriam; Poplawski, Nicola; Verlee, Maxim; Humphreys, David T; Harvey, Richard P; Chapman, Gavin; Kirk, Edwin P; Winlaw, David S; Callewaert, Bert; Chung, Wendy K; Ascher, David; Giannoulatou, Eleni; Dunwoodie, Sally L