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APA Citation
Hovden, S., Rejnmark, L., Ladefoged, S. A., & Nissen, P. H. (2017). aP2S1 and GNA11 mutations – not a common cause of familial hypocalciuric hypercalcemia. European journal of endocrinology, 176(2), 177–185. http://access.bl.uk/ark:/81055/vdc_100039857714.0x000012