Home
About
Overview
Sharing Data
ORCID
Help
History (1)
A novel mutation in HSD11B2 causes apparent mineralocorticoid excess in an Omani kindred.
See All Pages
Find People
Find Everything
Login
to edit your profile (add a photo, awards, links to other websites, etc.)
Edit My Profile
My Person List (
0
)
Return to Top
A novel mutation in HSD11B2 causes apparent mineralocorticoid excess in an Omani kindred.
A novel mutation in HSD11B2 causes apparent mineralocorticoid excess in an Omani kindred. Ann N Y Acad Sci. 2016 07; 1376(1):65-71.
View in:
PubMed
subject areas
11-beta-Hydroxysteroid Dehydrogenase Type 2
Amino Acid Sequence
Base Sequence
Child, Preschool
Computer Simulation
DNA Mutational Analysis
Family
Female
Follow-Up Studies
Humans
Infant
Infant, Newborn
Male
Mineralocorticoid Excess Syndrome, Apparent
Models, Molecular
Mutation
Oman
authors with profiles
Robert C Wilson