Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism. (2018)

First Author: Cangul H

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