Publication | Closed Access
Mutations in the human Ca2+-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism
1K
Citations
27
References
1993
Year
GeneticsPhysiologyNeonatal Severe HyperparathyroidismParathyroid HormoneParathyroid DiseaseParathyroid GlandFamilial Hypocalciuric Hypercalcemia
| Year | Citations | |
|---|---|---|
Page 1
Page 1