Silje Hovden

AP2S1 and GNA11 mutations - not a common cause of familial hypocalciuric hypercalcemia.

L. Rejnmark, P. Nissen, S. Ladefoged, 2017, European journal of endocrinology.

Multiple endocrine neoplasia phenocopy revealed as a co‐occurring neuroendocrine tumor and familial hypocalciuric hypercalcemia type 3

L. Rejnmark, P. Poulsen, P. Nissen, 2016, Clinical case reports.