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

First Author: Peters C
Attributed to:  Confidence in Concept 2012 - Cambridge funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.17863/cam.39529

Publication URI: https://www.repository.cam.ac.uk/handle/1810/292379

Type: Journal Article/Review