Biallelic mutations in CYP24A1 or SLC34A1 as a cause of infantile idiopathic hypercalcemia (IIH) with vitamin D hypersensitivity: molecular study of 11 historical IIH casesEwa Pronicka, Mieczysław Litwin, Paulina Halat et al.|Journal of Applied Genetics|2017Cited by 94