Brief Report: A Novel Sodium/Iodide Symporter Mutation, S356F, Causing Congenital Hypothyroidism. (2022)

First Author: Durgia H
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