Publication | Closed Access
Stepwise CaSR, AP2S1, and GNA11 sequencing in patients with suspected familial hypocalciuric hypercalcemia
32
Citations
20
References
2017
Year
Stepwise CasrMendelian DisorderGenetic DisorderMedicineGeneticsInherited Metabolic DiseaseGenetic EpidemiologyPathologyMolecular GeneticsMolecular DiagnosticsEpigeneticsClinical Genetics
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