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/10.1089/thy.2021.0478
PubMed Identifier: 34806438
Publication URI: http://europepmc.org/abstract/MED/34806438
Type: Journal Article/Review
Volume: 32
Parent Publication: Thyroid : official journal of the American Thyroid Association
Issue: 2
ISSN: 1050-7256