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