Cite
HARVARD Citation
Aashiq, M. et al. (2020). Clinical and Biochemical Features in a Case of Familial Hypocalciuric Hypercalcemia Type 3 with AP2S1 Gene Mutation in Codon Arg15His. Case reports in pediatrics. p. . [Online].
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Aashiq, M. et al. (2020). Clinical and Biochemical Features in a Case of Familial Hypocalciuric Hypercalcemia Type 3 with AP2S1 Gene Mutation in Codon Arg15His. Case reports in pediatrics. p. . [Online].