Zhang, F., Zhang, L., He, L., Cao, M., Yang, Y., Duan, X., . . . Liu, K. (2021). A PITX2 splice-site mutation in a family with Axenfeld-Rieger syndrome leads to decreased expression of nuclear PITX2 protein. Int Ophthalmol.
Stile di citazione ChicagoZhang, Feng, Lusi Zhang, Li He, Mengdan Cao, Yuting Yang, Xuanchu Duan, Jingming Shi, e Ke Liu. "A PITX2 Splice-site Mutation in a Family With Axenfeld-Rieger Syndrome Leads to Decreased Expression of Nuclear PITX2 Protein." Int Ophthalmol 2021.
Citazione MLAZhang, Feng, et al. "A PITX2 Splice-site Mutation in a Family With Axenfeld-Rieger Syndrome Leads to Decreased Expression of Nuclear PITX2 Protein." Int Ophthalmol 2021.
Attenzione: Queste citazioni potrebbero non essere precise al 100%.