Brief Report: A Novel Sodium/Iodide Symporter Mutation, S356F, Causing Congenital Hypothyroidism. (2022)
Attributed to:
Enabling technologies
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.17863/cam.76715
Publication URI: https://www.repository.cam.ac.uk/handle/1810/329265
Type: Journal Article/Review