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DUOX2/DUOXA2 Mutations Frequently Cause Congenital Hypothyroidism that Evades Detection on Newborn Screening in the United Kingdom. (2019)

First Author: Peters C

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