Cole DEC, Janicic N, Salisbury SR, Hendy GN (1997): Neonatal severe hyperparathyroidism, secondary hyperparathyroidism, and familial hypocalciuric hypercalcemia: Multiple different phenotypes associated with an inactivating Alu insertion mutation of the calcium‐sensing receptor gene. Am J Med Genet 71:202‐210.

The authors of the article referenced above have revised Figure 1A. Below is the correct version of the figure.In addition, the authors would like to replace the following sentence which appears on line 14 of page 208 in the Section, Secondary Hyperparathyroidism. The authors regret these errors.