HY, M., NN, W., & SO, O. (2025). Familial hypocalciuric hypercalcaemia type 1 due to a rare CASR missense mutation: A delayed diagnosis in a man with chronic hypercalcaemia. BMJ case reports, 18(9), . https://doi.org/10.1136/bcr-2025-266308
Chicago Style (17th ed.) CitationHY, Mon, Win NN, and Oyibo SO. "Familial Hypocalciuric Hypercalcaemia Type 1 Due to a Rare CASR Missense Mutation: A Delayed Diagnosis in a Man with Chronic Hypercalcaemia." BMJ Case Reports 18, no. 9 (2025). https://doi.org/10.1136/bcr-2025-266308.
MLA (9th ed.) CitationHY, Mon, et al. "Familial Hypocalciuric Hypercalcaemia Type 1 Due to a Rare CASR Missense Mutation: A Delayed Diagnosis in a Man with Chronic Hypercalcaemia." BMJ Case Reports, vol. 18, no. 9, 2025, https://doi.org/10.1136/bcr-2025-266308.