Hong, N., Zhang, E., Wang, Q., Zhang, X., Li, F., Fu, Q., . . . Sun, K. (2018). A loss-of-function mutation p.T52S in RIPPLY3 is a potential predisposing genetic risk factor for Chinese Han conotruncal heart defect patients without the 22q11.2 deletion/duplication. J Transl Med.
Stile di citazione ChicagoHong, Nanchao, et al. "A Loss-of-function Mutation P.T52S in RIPPLY3 Is a Potential Predisposing Genetic Risk Factor for Chinese Han Conotruncal Heart Defect Patients Without the 22q11.2 Deletion/duplication." J Transl Med 2018.
Citazione MLAHong, Nanchao, et al. "A Loss-of-function Mutation P.T52S in RIPPLY3 Is a Potential Predisposing Genetic Risk Factor for Chinese Han Conotruncal Heart Defect Patients Without the 22q11.2 Deletion/duplication." J Transl Med 2018.