Pronicka, E., Ciara, E., Halat, P., Janiec, A., Wójcik, M., Rowińska, E., . . . Litwin, M. (2017). Biallelic mutations in CYP24A1 or SLC34A1 as a cause of infantile idiopathic hypercalcemia (IIH) with vitamin D hypersensitivity: Molecular study of 11 historical IIH cases. J Appl Genet.
Chicago ZitierstilPronicka, Ewa, et al. "Biallelic Mutations in CYP24A1 or SLC34A1 As a Cause of Infantile Idiopathic Hypercalcemia (IIH) With Vitamin D Hypersensitivity: Molecular Study of 11 Historical IIH Cases." J Appl Genet 2017.
MLA ZitierstilPronicka, Ewa, et al. "Biallelic Mutations in CYP24A1 or SLC34A1 As a Cause of Infantile Idiopathic Hypercalcemia (IIH) With Vitamin D Hypersensitivity: Molecular Study of 11 Historical IIH Cases." J Appl Genet 2017.