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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.

scientific article published on 3 May 2017

Author/s

author: Ewa Pronicka, Elżbieta Ciara, Marek Wojcik, Dariusz Rokicki, Paweł Płudowski, Aldona Wierzbicka-Rucińska, Janusz Ksiazyk, Mieczyslaw Litwin, Paulina Halat-Wolska, Agnieszka Koppolu

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Work details

Publication date
May 3, 2017
- -
Language
English

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