DUOX2/DUOXA2 Mutations Frequently Cause Congenital Hypothyroidism that Evades Detection on Newborn Screening in the United Kingdom. (2019)
Attributed to:
Enabling technologies
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1089/thy.2018.0587
PubMed Identifier: 31044655
Publication URI: http://europepmc.org/abstract/MED/31044655
Type: Journal Article/Review
Volume: 29
Parent Publication: Thyroid : official journal of the American Thyroid Association
Issue: 6
ISSN: 1050-7256