Harvard Catalyst Profiles
Contact, publication, and social network information about Harvard faculty and fellows.
Open Source Software
to edit your profile (add a photo, awards, links to other websites, etc.)
Edit My Profile
My Person List (
Login and Edit functionaility are currrently unavailable.
Return to Top
Search Result Details
Back to Search Results
This page shows the details of why an item matched the keywords from your search.
One or more keywords matched the following items that are connected to
Congenital Disorders of Glycosylation
Defining the phenotype in congenital disorder of glycosylation due to ALG1 mutations.
B4GALT1-congenital disorders of glycosylation presents as a non-neurologic glycosylation disorder with hepatointestinal involvement.
Congenital disorders of glycosylation--a challenging group of IEMs.
A novel FAM20C mutation causes a rare form of neonatal lethal Raine syndrome.
An emerging role for endothelial barrier support therapy for congenital disorders of glycosylation.