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A rare case of familial Cushing's syndrome with a common presentation of weight gain due to a mutation of the PRKAR1A gene causing isolated primary pigmented nodular adrenocortical disease

Bibliographic reference Poukoulidou, Thekla ; Maiter, Dominique ; Bertherat, Jerome ; Beauloye, Véronique. A rare case of familial Cushing's syndrome with a common presentation of weight gain due to a mutation of the PRKAR1A gene causing isolated primary pigmented nodular adrenocortical disease. In: Journal of Pediatric Endocrinology & Metabolism, Vol. 27, no. 9-10, p. 1005-1009 (2014)
Permanent URL http://hdl.handle.net/2078.1/151294