Home
About
Overview
Sharing Data
ORCID
Help
History (1)
A novel mechanism of inherited TBG deficiency: mutation in a liver-specific enhancer.
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 mechanism of inherited TBG deficiency: mutation in a liver-specific enhancer.
A novel mechanism of inherited TBG deficiency: mutation in a liver-specific enhancer. J Clin Endocrinol Metab. 2015 Jan; 100(1):E173-81.
View in:
PubMed
subject areas
Adolescent
Adult
Child
Enhancer Elements, Genetic
Female
Haplotypes
Humans
Liver
Male
Middle Aged
Mutation
Pedigree
Thyroid Diseases
Thyroxine-Binding Globulin
Young Adult
authors with profiles
Christopher D. Brown
Samuel Refetoff
Alexandra M. Dumitrescu
Roy Emanuel Weiss
Marcelo A. Nobrega