Home
About
Overview
Sharing Data
ORCID
Help
History (1)
Absence of mutations in HCRT, HCRTR1 and HCRTR2 in patients with ROHHAD.
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
Absence of mutations in HCRT, HCRTR1 and HCRTR2 in patients with ROHHAD.
Absence of mutations in HCRT, HCRTR1 and HCRTR2 in patients with ROHHAD. Respir Physiol Neurobiol. 2016 Jan 15; 221:59-63.
View in:
PubMed
subject areas
Autonomic Nervous System Diseases
Child
Female
Humans
Hypothalamic Diseases
Mutation
Obesity Hypoventilation Syndrome
Orexin Receptors
Orexins
authors with profiles
Elizabeth Berry-Kravis