Bhanot, M., Ramirez, A., & Dahir, K. (2019). SAT-506 Identification of a Mutation in AP2S1 Causing Familial Hypocalciuric Hypercalcemia Type 3 in a Patient with Unknown Family History of the Disease. J Endocr Soc.
Παραπομπή Chicago StyleBhanot, Monica, Andrea Ramirez, και Kathryn Dahir. "SAT-506 Identification of a Mutation in AP2S1 Causing Familial Hypocalciuric Hypercalcemia Type 3 in a Patient With Unknown Family History of the Disease." J Endocr Soc 2019.
Παραπομπή MLABhanot, Monica, Andrea Ramirez, και Kathryn Dahir. "SAT-506 Identification of a Mutation in AP2S1 Causing Familial Hypocalciuric Hypercalcemia Type 3 in a Patient With Unknown Family History of the Disease." J Endocr Soc 2019.
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