Clinical and Biochemical Features in a Case of Familial...

Case Reports in Pediatrics 2020 / 01 Vol. 2020

Clinical and Biochemical Features in a Case of Familial Hypocalciuric Hypercalcemia Type 3 with AP2S1 Gene Mutation in Codon Arg15His

Aashiq, Mohamed, Malallah, Asma Jassim, Khan, Farheen, Alsada, Maryam
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Volume:
2020
Journal:
Case Reports in Pediatrics
DOI:
10.1155/2020/7312894
Date:
January, 2020
File:
PDF, 1.11 MB
2020
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