APA Alıntı

Kerut, S., Kovvuru, K. R., Yanes-Cardozo, L., & Garla, V. V. (2020). Familial hypocalciuric hypercalcaemia type 3: AP2S1 missense mutation. BMJ Case Rep.

Chicago Stili Alıntı

Kerut, Sarah, Karthik Reddy Kovvuru, Licy Yanes-Cardozo, ve Vishnu Vardhan Garla. "Familial Hypocalciuric Hypercalcaemia Type 3: AP2S1 Missense Mutation." BMJ Case Rep 2020.

MLA Alıntı

Kerut, Sarah, Karthik Reddy Kovvuru, Licy Yanes-Cardozo, ve Vishnu Vardhan Garla. "Familial Hypocalciuric Hypercalcaemia Type 3: AP2S1 Missense Mutation." BMJ Case Rep 2020.