Clinical, genetic, and structural basis of apparent mineralocorticoid excess due to 11β-hydroxysteroid dehydrogenase type 2 deficiency.

Autor: Yau, Mabel, Khattab, Ahmed, Newa, Maria I., Haider, Shozeb, Chen Ling, Ewert, Sinead, Mudryi, Vitalii, Alzubdi, Mouch, Mathew, Mehr, Bloch, Madison, Patel, Monica, Toygar, Aysenur, Ozdemir, Hatice Nur, Abu-Amer, Wahid, Li Sun, Se-Min Kim, Yuen, Tony, Zaidi, Mone, Zaidi, Samir, Abdullah, Wafa

Publikováno v: Proceedings of the National Academy of Sciences of the United States of America; 12/26/2017, Vol. 114 Issue 52, p11248-11256, 9p