Publication | Closed Access
Severe hypercalcemic crisis in an infant with idiopathic infantile hypercalcemia caused by mutation in CYP24A1 gene
59
Citations
11
References
2012
Year
Mendelian DisorderGenetic DisorderCyp24a1 GenePhysiologyInherited Metabolic DiseasePediatricsPathologySevere Hypercalcemic CrisisIdiopathic Infantile HypercalcemiaMedicine
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