Cite
HARVARD Citation
Hovden, S. et al. (2017). AP2S1 and GNA11 mutations – not a common cause of familial hypocalciuric hypercalcemia. European journal of endocrinology. 176 (2), pp. 177-185. [Online].
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Hovden, S. et al. (2017). AP2S1 and GNA11 mutations – not a common cause of familial hypocalciuric hypercalcemia. European journal of endocrinology. 176 (2), pp. 177-185. [Online].