APA

Xekouki P., Hatch M. M., Lin L., Rodrigo D. A., Azevedo M., de la Luz Sierra M., Levy I., Saloustros E., Moraitis A., Horvath A., Kebebew E., Hoffman D. A. & Stratakis C. A. (20120907). KCNJ5 mutations in the National Institutes of Health cohort of patients with primary hyperaldosteronism: an infrequent genetic cause of Conn's syndrome. : Endocrine-related cancer.

Chicago

Xekouki Paraskevi, Hatch Michael M, Lin Lin, Rodrigo De Alexandre, Azevedo Monalisa, de la Luz Sierra Maria, Levy Isaac, Saloustros Emmanouil, Moraitis Andreas, Horvath Anelia, Kebebew E, Hoffman Dax A and Stratakis Constantine A. 20120907. KCNJ5 mutations in the National Institutes of Health cohort of patients with primary hyperaldosteronism: an infrequent genetic cause of Conn's syndrome. : Endocrine-related cancer.

Harvard

Xekouki P., Hatch M. M., Lin L., Rodrigo D. A., Azevedo M., de la Luz Sierra M., Levy I., Saloustros E., Moraitis A., Horvath A., Kebebew E., Hoffman D. A. and Stratakis C. A. (20120907). KCNJ5 mutations in the National Institutes of Health cohort of patients with primary hyperaldosteronism: an infrequent genetic cause of Conn's syndrome. : Endocrine-related cancer.

MLA

Xekouki Paraskevi, Hatch Michael M, Lin Lin, Rodrigo De Alexandre, Azevedo Monalisa, de la Luz Sierra Maria, Levy Isaac, Saloustros Emmanouil, Moraitis Andreas, Horvath Anelia, Kebebew E, Hoffman Dax A and Stratakis Constantine A. KCNJ5 mutations in the National Institutes of Health cohort of patients with primary hyperaldosteronism: an infrequent genetic cause of Conn's syndrome. : Endocrine-related cancer. 20120907.