APA (7th ed.) Citation

Mannstadt, M., Nesbit, M., Howles, S., Rogers, A., Thakker, R., & Jueppner, H. (2013). Gain-of-Function Mutations in G alpha 11 Cause a Novel Form of Autosomal-Dominant Hypoparathyroidism.

Chicago Style (17th ed.) Citation

Mannstadt, M., M. Nesbit, S. Howles, A. Rogers, R. Thakker, and H. Jueppner. Gain-of-Function Mutations in G Alpha 11 Cause a Novel Form of Autosomal-Dominant Hypoparathyroidism. 2013.

MLA (9th ed.) Citation

Mannstadt, M., et al. Gain-of-Function Mutations in G Alpha 11 Cause a Novel Form of Autosomal-Dominant Hypoparathyroidism. 2013.