M, F., Y, L., K, X., L, G., & Q, P. (2026). A novel gain-of-function mutation (W818R) of calcium-sensing receptor in a family with autosomal dominant hypocalcemia type 1. Frontiers in endocrinology, 17, 1806677. https://doi.org/10.3389/fendo.2026.1806677
Chicago Style (17th ed.) CitationM, Fu, Luo Y, Xu K, Guo L, and Pan Q. "A Novel Gain-of-function Mutation (W818R) of Calcium-sensing Receptor in a Family with Autosomal Dominant Hypocalcemia Type 1." Frontiers in Endocrinology 17 (2026): 1806677. https://doi.org/10.3389/fendo.2026.1806677.
MLA (9th ed.) CitationM, Fu, et al. "A Novel Gain-of-function Mutation (W818R) of Calcium-sensing Receptor in a Family with Autosomal Dominant Hypocalcemia Type 1." Frontiers in Endocrinology, vol. 17, 2026, p. 1806677, https://doi.org/10.3389/fendo.2026.1806677.