A Novel Homozygous Missense Mutation of the Dual Oxidase 2 (DUOX2) Gene in an Adult Patient with Large Goiter
Author:
Affiliation:
1. Department of Internal Medicine, Kuma Hospital, Kobe, Japan.
2. Department of Clinical Laboratory Medicine, Dokkyo Medical University, Mibu, Japan.
3. Department of Surgery, Kuma Hospital, Kobe, Japan.
Publisher
Mary Ann Liebert Inc
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Link
https://www.liebertpub.com/doi/pdf/10.1089/thy.2007.0258
Reference22 articles.
1. The genetics of euthyroid familial goiter
2. Genetics of congenital hypothyroidism
3. An Outline of Inherited Disorders of the Thyroid Hormone Generating System
4. Mutations in the sodium/iodide symporter (NIS) gene as a cause for iodide transport defects and congenital hypothyroidism
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