Clinical, genetic, and structural basis of apparent mineralocorticoid excess due to 11β-hydroxysteroid dehydrogenase type 2 deficiency
Yau, Mabel, Haider, Shozeb, Khattab, Ahmed, Ling, Chen, Mathew, Mehr, Zaidi, Samir, Bloch, Madison, Patel, Monica, Ewert, Sinead, Abdullah, Wafa, Toygar, Aysenur, Mudryi, Vitalii, Badi, Maryam Al, Alzubdi, Mouch, Wilson, Robert C., Azkawi, Hanan Said Al, Ozdemir, Hatice Nur, Abu-Amer, Wahid, Hertecant, Jozef, Razzaghy-Azar, Maryam, Funder, John W., Senani, Aisha Al, Sun, Li, Kim, Se-Min, Yuen, Tony, Zaidi, Mone, New, Maria I.
Published in Proceedings of the National Academy of Sciences - PNAS (26.12.2017)
Published in Proceedings of the National Academy of Sciences - PNAS (26.12.2017)
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Journal Article
A novel mutation in HSD11B2 causes apparent mineralocorticoid excess in an Omani kindred
Yau, Mabel, Azkawi, Hanan Said Al, Haider, Shozeb, Khattab, Ahmed, Badi, Maryam Al, Abdullah, Wafa, Senani, Aisha Al, Wilson, Robert C., Yuen, Tony, Zaidi, Mone, New, Maria I.
Published in Annals of the New York Academy of Sciences (01.07.2016)
Published in Annals of the New York Academy of Sciences (01.07.2016)
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Journal Article
Clinical, genetic, and structural basis of apparent mineralocorticoid excess due to 11ß- hydroxysteroid dehydrogenase type 2 deficiency
Yau, Mabel, Haider, Shozeb, Khattab, Ahmed, Ling, Chen, Mathew, Mehr, Zaidi, Samir, Bloch, Madison, Patel, Monica, Ewert, Sinead, Abdullah, Wafa, Toygar, Aysenur, Mudryi, Vitalii, Badi, Maryam Al, Alzubdi, Mouch, Wilson, Robert C, Al Azkawi, Hanan Said, Ozdemir, Hatice Nur, Abu-Amer, Wahid, Hertecant, Jozef, Razzaghy-Azar, Maryam, Funder, John W, Al Senani, Aisha, Sun, Li, Kim, Se-Min, Yuen, Tony, Zaidi, Mone, New, Maria I
Published in Proceedings of the National Academy of Sciences - PNAS (26.12.2017)
Get full text
Published in Proceedings of the National Academy of Sciences - PNAS (26.12.2017)
Journal Article