Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism. (2018)
Attributed to:
Enabling technologies
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1172/jci.insight.99631
PubMed Identifier: 30333321
Publication URI: http://europepmc.org/abstract/MED/30333321
Type: Journal Article/Review
Volume: 3
Parent Publication: JCI insight
Issue: 20
ISSN: 2379-3708