ArticleJournal of applied genetics2017
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.
Ewa Pronicka et al.PubMed ↗Full text ↗Publisher ↗
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