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Clinical, genetic, and structural basis of apparent mineral..:

Yau, Mabel ; Haider, Shozeb ; Khattab, Ahmed...
Proceedings of the National Academy of Sciences of the United States of America. 114 (2017) 52 - p. E11248-E11256 , 2017

Link: https://www.jstor.org/stable/26488808

RT Journal
T1 <Title>Clinical, genetic, and structural basis of apparent mineralocorticoid excess due to 11β-hydroxysteroid dehydrogenase type 2 deficiency</Title>

UL https://suche.suub.uni-bremen.de/peid=jstor-26488808&Exemplar=1&LAN=DE
				
A1 Yau, Mabel
A1 Haider, Shozeb
A1 Khattab, Ahmed
A1 Ling, Chen
A1 Mathew, Mehr
A1 Zaidi, Samir
A1 Bloch, Madison
A1 Patel, Monica
A1 Ewert, Sinead
A1 Abdullah, Wafa
A1 Toygar, Aysenur
A1 Mudryi, Vitalii
A1 Badi, Maryam Al
A1 Alzubdi, Mouch
A1 Wilson, Robert C.
A1 Azkawi, Hanan Said Al
A1 Ozdemir, Hatice Nur
A1 Abu-Amer, Wahid
A1 Hertecant, Jozef
A1 Razzaghy-Azar, Maryam
A1 Funder, John W.
A1 Senani, Aisha Al
A1 Sun, Li
A1 Kim, Se-Min
A1 Yuen, Tony
A1 Zaidi, Mone
A1 New, Maria I.
PB National Academy of Sciences
YR 2017
SN 0027-8424
SN 1091-6490
K1 in silico molecular modeling
K1 molecular dynamics
K1 hypertension
K1 congenital adrenal hyperplasia
JF Proceedings of the National Academy of Sciences of the United States of America
VO 114
IS 52
SP E11248
OP E11256
LK http://dx.doi.org/https://www.jstor.org/stable/26488808
DO https://www.jstor.org/stable/26488808
SF ELIB - SuUB Bremen

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